Food Labeling; Revision of the Nutrition and Supplement Facts Labels; Technical Amendments, 65493-65506 [2018-27431]

Download as PDF Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations Appendix G to Part 91—Operations in Reduced Vertical Separation Minimum (RVSM) Airspace Section 1. Definitions Reduced Vertical Separation Minimum (RVSM) Airspace. Within RVSM airspace, air traffic control (ATC) separates aircraft by a minimum of 1,000 feet vertically between FL 290 and FL 410 inclusive. Air-traffic control notifies operators of RVSM airspace by providing route planning information. * * * * * Section 2. Aircraft Approval (a) Except as specified in Section 9 of this appendix, an operator may be authorized to conduct RVSM operations if the Administrator finds that its aircraft comply with this section. * * * * (a) Except as specified in Section 9 of this appendix, authority for an operator to conduct flight in airspace where RVSM is applied is issued in operations specifications, a Letter of Authorization, or management specifications issued under subpart K of this part, as appropriate. To issue an RVSM authorization under this section, the Administrator must find that the operator’s aircraft have been approved in accordance with Section 2 of this appendix and the operator complies with this section. (b) Except as specified in Section 9 of this appendix, an applicant seeking authorization to operate within RVSM airspace must apply in a form and manner prescribed by the Administrator. The application must include the following: * * * * (c) In a manner prescribed by the Administrator, an operator seeking authorization under this section must provide evidence that: * * * * * (2) Each pilot has knowledge of RVSM requirements, policies, and procedures sufficient for the conduct of operations in RVSM airspace. Section 4. RVSM Operations amozie on DSK3GDR082PROD with RULES * * * * * (b) * * * (1) The operator is authorized by the Administrator to perform such operations in accordance with Section 3 or Section 9 of this appendix, as applicable. (2) The aircraft— (i) Has been approved and complies with Section 2 this appendix; or (ii) Complies with Section 9 of this appendix. (3) Each pilot has knowledge of RVSM requirements, policies, and procedures sufficient for the conduct of operations in RVSM airspace. Section 5. Deviation Authority Approval The Administrator may authorize an aircraft operator to deviate from the requirements of §§ 91.180 or 91.706 for a specific flight in RVSM airspace if— * * * VerDate Sep<11>2014 * * 16:23 Dec 20, 2018 * * * * * Jkt 247001 44701(a) in Washington, DC, on December 10, 2018. Daniel K. Elwell, Acting Administrator. [FR Doc. 2018–27401 Filed 12–20–18; 8:45 am] BILLING CODE 4910–13–P Section 7. Removal or Amendment of Authority The Administrator may prohibit or restrict an operator from conducting operations in RVSM airspace, if the Administrator determines that the operator is not complying, or is unable to comply, with this appendix or subpart H of this part. Examples of reasons for amendment, revocation, or restriction include, but are not limited to, an operator’s: * * * * * Section 8. Airspace Designation * Section 3. Operator Authorization * (b) At the time of filing the flight plan for that flight, ATC determines that the aircraft may be provided appropriate separation and that the flight will not interfere with, or impose a burden on, RVSM operations. 65493 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 101 [Docket No. FDA–2012–N–1210] Food Labeling; Revision of the Nutrition and Supplement Facts Labels; Technical Amendments RVSM may be applied in all ICAO Flight Information Regions (FIRs). AGENCY: Section 9. Aircraft Equipped With Automatic Dependent Surveillance—Broadcast Out ACTION: An operator is authorized to conduct flight in airspace in which RVSM is applied provided: (a) The aircraft is equipped with the following: (1) Two operational independent altitude measurement systems. (2) At least one automatic altitude control system that controls the aircraft altitude— (i) Within a tolerance band of ±65 feet about an acquired altitude when the aircraft is operated in straight and level flight under nonturbulent, nongust conditions; or (ii) Within a tolerance band of ±130 feet under nonturbulent, nongust conditions for aircraft for which application for type certification occurred on or before April 9, 1997, that are equipped with an automatic altitude control system with flight management/performance system inputs. (3) An altitude alert system that signals an alert when the altitude displayed to the flightcrew deviates from the selected altitude by more than— (i) ±300 feet for aircraft for which application for type certification was made on or before April 9, 1997; or (ii) ±200 feet for aircraft for which application for type certification is made after April 9, 1997. (4) A TCAS II that meets TSO C–119b (Version 7.0), or a later version, if equipped with TCAS II, unless otherwise authorized by the Administrator. (5) Unless authorized by ATC or the foreign country where the aircraft is operated, an ADS–B Out system that meets the equipment performance requirements of § 91.227 of this part. The aircraft must have its height-keeping performance monitored in a form and manner acceptable to the Administrator. (b) The altimetry system error (ASE) of the aircraft does not exceed 200 feet when operating in RVSM airspace. Issued under authority provided by 49 U.S.C. 106(f), 40103(b), 40113(a), and PO 00000 Frm 00009 Fmt 4700 Sfmt 4700 Food and Drug Administration, HHS. Final rule; technical amendment. The Food and Drug Administration (FDA or we) is amending the regulations pertaining to the Nutrition Facts and Supplement Facts labels. The amendments correct errors that were made in labeling examples, restore incorrect deletions, correct the edition of a reference cited in the rule, and correct cross-references to other regulations. This action is ministerial or editorial in nature. DATES: This rule is effective December 21, 2018. FOR FURTHER INFORMATION CONTACT: Mark Kantor, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, 240–402–2082. SUPPLEMENTARY INFORMATION: SUMMARY: I. Background In the Federal Register of May 27, 2016 (81 FR 33742 and 81 FR 34000), we published two final rules entitled ‘‘Food Labeling: Revision of the Nutrition and Supplement Facts Labels’’ (the Nutrition Facts Label Final Rule) and ‘‘Food Labeling: Serving Sizes of Foods That Can Reasonably Be Consumed At One Eating Occasion; Dual-Column Labeling; Updating, Modifying, and Establishing Certain Reference Amounts Customarily Consumed; Serving Size for Breath Mints; and Technical Amendments’’ (the Serving Size Final Rule). The Nutrition Facts Label Final Rule revises the Nutrition Facts label by: • Removing the declaration of ‘‘Calories from fat’’ because current science supports a view that the type of fat is more relevant than overall total fat intake in increased risk of chronic diseases; E:\FR\FM\21DER1.SGM 21DER1 amozie on DSK3GDR082PROD with RULES 65494 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations • requiring the declaration of the gram amount of ‘‘added sugars’’ in a serving of a product, establishing a Daily Reference Value (DRV), and requiring the percent Daily Value (DV) declaration for added sugars; • changing ‘‘Sugars’’ to ‘‘Total Sugars’’ and requiring that ‘‘Includes ‘X’ g Added Sugars’’ be indented and declared directly below ‘‘Total Sugars’’ on the label; • updating the list of vitamins and minerals of public health significance. For example, the Nutrition Facts Label Final Rule requires the declaration of vitamin D and potassium and permits, rather than requires, the declaration of vitamins A and C; • updating certain reference values used in the declaration of percent DVs of nutrients on the Nutrition Facts and Supplement Facts labels; • revising the format of the Nutrition Facts label to increase the prominence of the term ‘‘Calories;’’ • removing the requirement for the footnote table listing the reference values for certain nutrients for 2,000 and 2,500 calorie diets; • requiring the maintenance of records to support the declarations of certain nutrients under specified circumstances. For example, because there are no analytical methods that can distinguish between dietary fiber (soluble and insoluble fiber) and nondigestible carbohydrates that do not meet the definition of dietary fiber; added and naturally occurring sugars or the various forms of vitamin E; or folate and folic acid, the Nutrition Facts Label Final Rule requires manufacturers to make and keep certain written records to verify the declarations of dietary fiber, added sugars, vitamin E, and folate and folic acid in the labeling of the food associated with such records. The Nutrition Facts Label Final Rule requires these records to be kept for at least 2 years after introduction or delivery for introduction of the food into interstate commerce. A similar requirement exists with respect to added sugars in foods subject to nonenzymatic browning and fermentation because there are no analytical methods that can determine the amount of added sugar in specific foods containing added sugars alone or in combination with naturally occurring sugars, where the added sugars are subject to nonenzymatic browning and fermentation. However, for manufacturers of such foods who are unable to reasonably approximate the amount of added sugars in a serving of food to which the records requirements apply, the Nutrition Facts Label Final Rule allows manufacturers to submit a petition to request an alternative means of compliance; and • establishing a compliance date of 2 years after the Nutrition Facts Label Final Rule’s effective date, except that manufacturers with less than $10 million in annual food sales have a compliance date of 3 years after the Nutrition Facts Label Final Rule’s effective date. (In the Federal Register of May 4, 2018 (83 FR 19619), however, we extended the compliance date for manufacturers with $10 million or more in annual food sales from July 26, 2018, to January 1, 2020, and the compliance date for manufacturers with less than $10 million in annual food sales from July 26, 2019, to January 1, 2021.) VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 The Serving Size Final Rule requires all containers, including containers of products with ‘‘large’’ reference amounts customarily consumed (RACCs) (i.e., products with RACCs of at least 100 grams (g) or 100 milliliters (mL)), containing less than 200 percent of the RACC to be labeled as a singleserving container. Except for when certain exceptions apply, the Serving Size Final Rule further requires that containers and units that contain at least 200 percent and up to and including 300 percent of the RACC be labeled with a column of nutrition information within the Nutrition Facts label that lists the quantitative amounts and percent DVs for the entire container, in addition to the required column listing the quantitative amounts and percent DVs for a serving that is less than the entire container (i.e., the serving size derived from the RACC). The Serving Size Final Rule also updates, modifies, and establishes RACCs for certain foods and product categories. II. Description of the Technical Amendments Since we published the two final rules in the Federal Register, we have noted or have been made aware of errors that appeared in the final rules. Most errors are non-substantive; for example, § 101.9(e)(5) and (6) (21 CFR 101.9(e)(5) and (6)) show sample Nutrition Facts labels. The sample labels, however, differed from the other sample labels in the Nutrition Facts Label Final Rule in that the line underneath ‘‘Saturated Fat’’ did not extend completely to the left edge of the label. Through this technical amendment, we are revising the sample labels so that the line extends completely to the left edge of the label. Other errors reflected inconsistencies between the Nutrition Facts Label Final Rule’s requirements and sample labels. For example, one sample label omitted information regarding the number of servings per container and serving size; both information elements are required. Through this technical amendment, we are revising the sample label to include the missing information. Three errors resulted in the removal of preexisting provisions even though the Nutrition Facts Label Final Rule did not intend to remove those provisions. To the contrary, the preamble to the Nutrition Facts Label Final Rule discussed the provisions as still existing. Consequently, the technical amendment restores those provisions. Other errors pertained to crossreferences; in some instances, the Nutrition Facts Label Final Rule and the Serving Size Final Rule mistakenly referred to a different provision. In another instance, the Nutrition Facts Label Final Rule omitted a crossreference to another provision. The technical amendment corrects the crossreferences. PO 00000 Frm 00010 Fmt 4700 Sfmt 4700 We describe the amendments in more detail below. A. Section 101.9(b) and a CrossReference Section 101.9(b)(2)(i) provides, in part, the requirements for serving sizes for products in discrete units (e.g., muffins, sliced products, such as sliced bread, or individually packaged products within a multiserving package). The Serving Size Final Rule revised § 101.9(b)(2)(i) by removing paragraph (b)(2)(i)(E) (which had pertained to the serving size declaration of individual units in certain multiserving packages where the product has a reference amount of 100 grams (or milliliters) or larger) and redesignated paragraphs (b)(2)(i)(F) through (I) accordingly (see 81 FR 34000 at 34040). For example, § 101.9(b)(2)(i)(G) was redesignated as § 101.9(b)(2)(i)(F). However, the Serving Size Final Rule neglected to revise a reference to previous § 101.9(b)(2)(i)(G) that appears in § 101.9(b)(5)(vi) (which pertains to ounces as a common household measure, with an appropriate visual unit of measure, for products that naturally vary in size). Consequently, we are revising § 101.9(b)(5)(vi) to refer to § 101.9(b)(2)(i)(F). B. Section 101.9(c)(2) and Statements Regarding Saturated Fat, Trans Fat, Polyunsaturated Fat, and Monounsaturated Fat Section 101.9(c)(2) discusses how a statement of the number of grams of total fat in a serving must be expressed. Before we issued the Nutrition Facts Label Final Rule, § 101.9(c)(2) contained four subordinate paragraphs that discussed how the number of grams of saturated fat, trans fat, polyunsaturated fat, and monounsaturated fat must be expressed; these subordinate paragraphs were numbered as § 101.9(c)(2)(i) through (iv). The Nutrition Facts Label Final Rule did not amend or revise these subordinate paragraphs; to the contrary, in the preamble to the Nutrition Facts Label Final Rule, we either referred to them to describe an existing requirement or expressly stated that we did not intend to change them (see 81 FR 33742 at 33785, 33860). Nevertheless, after we published the Nutrition Facts Label Final Rule, we learned that § 101.9(c)(2)(i) through (iv) had been removed from the Code of Federal Regulations. Because we did not intend such a result, the technical amendment restores § 101.9(c)(2)(i) through (iv). E:\FR\FM\21DER1.SGM 21DER1 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations C. Section 101.9(c)(6)(i), Fiber, and a Cross-Reference Section 101.9(c)(6)(i) discusses, among other things, specific isolated or synthetic non-digestible carbohydrates that we have determined to have physiological effects that are beneficial to human health and that must be included in the calculation of the amount of dietary fiber. One such carbohydrate is psyllium husk, and the Nutrition Facts Label Final Rule contained a cross-reference to § 101.81(c)(2)(ii)(A)(6) (21 CFR 101.81(c)(2)(ii)(A)(6)). The cross-reference was in error. The correct cross-reference is § 101.81(c)(2)(ii)(B)(1), and so we have revised § 101.9(c)(6)(i) accordingly. D. Section 101.9(c)(6)(iii), Added Sugars, and Simplified Format Section 101.9(c)(6)(iii) discusses how the ‘‘added sugars’’ statement must appear. The provision states, among other things, that if a statement of the added sugars content is not required and, as a result, is not declared on the Nutrition Facts label, then the statement ‘‘Not a significant source of added sugars’’ must be placed at the bottom of the table of nutrient values. However, § 101.9(f) discusses when the declaration of nutrition information may be presented in a simplified format. In general, a simplified format may be used when a food product contains insignificant amounts of eight or more of specific nutrients; these nutrients include ‘‘added sugars.’’ Therefore, the technical amendment revises § 101.9(c)(6)(iii) by adding ‘‘Except as provided for in paragraph (f) of this section,’’ at the start of the sentence describing where the statement, ‘‘Not a significant source of added sugars,’’ must be placed. amozie on DSK3GDR082PROD with RULES E. Section 101.9(c)(8)(ii) and Quantitative Weight and § 101.9(c)(8)(iv) and Retinol Activity Equivalents (RAE) and the Order of Nutrients on the Nutrition Facts Label Section 101.9(c)(8) establishes requirements related to the disclosure of vitamins and minerals on the Nutrition Facts label. The rule, at § 101.9(c)(8)(ii), discusses the declaration of vitamins and minerals as a quantitative amount by weight and percent of the Reference Daily Intake (RDI). In the preamble to the proposed rule to revise the Nutrition Facts and Supplement Facts labels, we described the proposed rule as requiring the declaration of the absolute amounts for all mandatory and voluntary vitamins and minerals, in addition to the requirement for percent DV VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 declaration; we also said that an exception to the proposed requirement would be Nutrition Facts labels for foods in small packages that have a total surface area available to bear labeling of 40 or less square inches (79 FR 11880 at 11952, March 3, 2014). The preamble to the Nutrition Facts Label Final Rule noted the same exception for smaller packages (81 FR 33742 at 33946). However, the codified text inadvertently omitted the language creating the exception. Consequently, we are restoring the exception to § 101.9(c)(8)(ii) so that the declaration of quantitative weights for these vitamins and minerals are not required for labels described in § 101.9(j)(13). Additionally, § 101.9(c)(8)(ii) contains a sentence mentioning the statement of the amount per serving of the vitamins and minerals ‘‘as described in this paragraph.’’ To clarify the reference of ‘‘this paragraph,’’ the technical amendment revises ‘‘this paragraph’’ to read as ‘‘this paragraph (c)(8)(ii)’’. Our regulations, at § 101.9(c)(8)(iv), describe, among other things, the units of measure for certain vitamins and minerals. The rule lists the nutrients, their units of measure, and their RDIs in a table; for vitamin A, the unit of measure is in micrograms RAE. Footnote 2 to the table explains that RAE means retinol activity equivalents and that 1 microgram RAE equals 1 microgram retinol, 2 microgram supplemental b-carotene, 12 micrograms b-carotene, or 24 micrograms acarotene, or 24 micrograms bcryptoxanthin. In the preamble to the Nutrition Facts Label Final Rule, in response to a comment regarding the unit of measure for vitamin A, we explained that the conversions for microgram RAE were 1 retinol activity equivalent (mcg RAE) = 1 mcg retinol, 2 mcg supplemental bcarotene, 12 mcg of dietary b-carotene, or 24 mcg of other dietary provitamin A carotenoids (a-carotene or bcryptoxanthin) (81 FR 33742 at 33913) (emphasis added). However, we neglected to insert the word ‘‘dietary’’ before b-carotene, a-carotene, and bcryptoxanthin in footnote 2. The technical amendment inserts ‘‘dietary’’ before b-carotene, a-carotene, and b-cryptoxanthin in the footnote and also renumbers the footnote as footnote 3. The renumbering of the footnote is necessary because the technical amendment also revises the order of the nutrients in the table at 21 CFR 101.8(c)(8)(iv); the nutrients were supposed to be placed in order so that nutrients that must be disclosed on the label appear first. However, the Nutrition Facts Label Final Rule PO 00000 Frm 00011 Fmt 4700 Sfmt 4700 65495 inadvertently neglected to reorder the nutrients in the table to reflect the status of vitamin D, calcium, iron, and potassium as nutrients that must be disclosed. As a result of reordering the nutrients in the table, footnote 2 is now footnote 3. F. Section 101.9(d)(1)(iii) and Type Size Section 101.9(d)(1)(iii) establishes the type sizes for information on the Nutrition Facts label. Among other things, the regulation requires information required under § 101.9(d)(9) (regarding the footnote to the Nutrition Facts label) to be in a type size no smaller than 6 point. In the preamble to the Nutrition Facts Label Final Rule, we discussed how other information pertaining to ‘‘Amount per serving’’ and ‘‘% Daily Value’’ also would be required to be in a type size no smaller than 6 point (see 81 FR 33742 at 33944 (discussing the type size for ‘‘Amount per serving’’) and 81 FR 33742 at 33952 (discussing the type size for ‘‘% Daily Value’’)). However, the codified text at § 101.9(d)(1)(iii) omitted the paragraph designations for ‘‘Amount per serving’’ and ‘‘% Daily Value,’’ which are § 101.9(d)(4) and (6), respectively. Consequently, the technical amendment adds paragraphs (d)(4) and (6) to the information that must be in a type size no smaller than 6 point. G. Section 101.9(e)(5) and (6) and Corrections to Sample Labels Section 101.9(e)(5) and (6) show sample Nutrition Facts labels. The sample labels illustrate how dual column labels might appear. Some sample labels, however, differed from the other sample labels in the Nutrition Facts Label Final Rule in that the line underneath ‘‘Saturated Fat’’ did not extend completely to the left edge of the label. The technical amendment revises the sample labels so that the line extends completely to the left edge of the label. In § 101.9(e)(5), the revised sample label also changes the value for potassium from 45 mg to 40 mg because the declaration of potassium is to be expressed to the nearest 10 mg. increment. Additionally, in § 101.9(e)(6)(i), we have revised the title for one sample label from ‘‘Dual Column Display’’ to ‘‘Dual Column Display, Per Serving and Per Container.’’ This revised title should help distinguish this sample label from the other sample label in § 101.9(e)(6)(i). As for the other sample label titled ‘‘Dual Columns, Per Serving and Per Unit’’), the sample label inadvertently omitted information regarding the E:\FR\FM\21DER1.SGM 21DER1 65496 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations servings per container and serving size. The technical amendment revises the sample label for ‘‘Dual Columns, Per Serving and Per Unit’’ to include information on servings per container and serving size. In § 101.9(e)(6)(ii), the sample label appeared blurred or difficult to read when printed in the Federal Register. The technical amendment substitutes a better quality image for the sample label. There are no changes to the contents of the sample label itself. H. Section 101.9(j)(13) and Addresses or Phone Numbers for Obtaining Required Nutrition Information and the Exception for Certain Individual Serving Size Packages Section 101.9(j)(13)(i) discusses requirements for foods in small packages. The Nutrition Facts Label Final Rule revised § 101.9(j)(13)(i) so that the Nutrition Facts label on small packages would not be required to bear a footnote explaining what the ‘‘% Daily Value’’ means and manufacturers could voluntarily include an abbreviated footnote of ‘‘% DV = % Daily Value’’ in a type size no smaller than 6 point. In revising § 101.9(j)(13)(i), we did not intend to affect the preexisting paragraphs at § 101.9(j)(13)(i)(A), which pertains to the use of an address or telephone number where consumers can obtain required information, and § 101.9(j)(13)(i)(B), which pertains to an exception for certain individual serving size packages of food. After we issued the Nutrition Facts Label Final Rule, we were informed that both paragraphs (j)(13)(i)(A) and (B) had, nevertheless, been deleted. Because we did not intend such a result, we are restoring paragraphs (j)(13)(i)(A) and (B) to § 101.9(j)(13)(i) and also correcting an error in § 101.9(j)(13)(i)(B) by replacing the reference to ‘‘§ 101.2(c)(5)’’ with ‘‘§ 101.2(c)(2).’’ The correction is necessary because § 101.2(c)(5) does not exist, and the correct reference is to § 101.2(c)(2). amozie on DSK3GDR082PROD with RULES I. Section 101.36 and Corrections to the Spelling of Phosphorus, the Listing of Potassium, the Size of Calories, and a Cross-Reference Section 101.36(b)(2)(i)(B) (21 CFR 101.36(b)(2)(i)(B)) names dietary ingredients that are to be declared on the Supplement Facts label. The Nutrition Facts Label Final Rule incorrectly spelled phosphorus as ‘‘phosphorous,’’ so the technical amendment uses the correct spelling. Additionally, we have replaced ‘‘Vitamin A’’ with ‘‘vitamin A’’ for purposes of punctuation. VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 Section 101.36(b)(2)(ii)(B) discusses how the amounts of vitamins and minerals must be declared on the Supplement Facts label. In brief, the regulation states that the amounts of vitamins and minerals, excluding sodium and potassium, must be the amount of vitamin or mineral included in one serving of the product, using the units of measurement and levels of significance given in § 101.9(c)(8)(iv). The exclusion regarding potassium was based originally on the fact that there was no RDI value for potassium. The technical amendment deletes ‘‘and potassium’’ from the exclusion in § 101.36(b)(2)(ii)(B) because § 101.9(c)(8)(iv), among other things, does set forth the RDI, nomenclature, and unit of measure for potassium. Thus, because § 101.9(c)(8)(iv) sets forth an RDI and units of measure for potassium, the exclusion for potassium in § 101.36(b)(2)(ii)(B) is no longer appropriate. Section 101.36(e) discusses type sizes for certain information on the Supplement Facts label. The rule specifies a minimum type size for footnotes (among other things) and gives an example of a footnote statement. However, the example, ‘‘Percent Daily Values are based on a 2,000 calorie diet,’’ was missing a quotation mark. The technical amendment restores the missing quotation mark for the phrase ‘‘Percent Daily Values are based on a 2,000 calorie diet.’’ Additionally, § 101.36(e) contains a sentence specifying the font size for ‘‘Calories’’ and the heading ‘‘Calories’’ and the actual number of calories per serving. This sentence, however, should have been removed from the codified text because, as we stated in our response to comment 483 in the Nutrition Facts Label Final Rule, many dietary supplement products may contribute a negligible amount of calories (81 FR 33742 at 33939). We stated that the Nutrition Facts Label Final Rule does not require information about calories to be displayed in a larger type size or highlighted on any Supplement Facts labels (id.). Therefore, we are removing the sentence regarding the font size and highlighting for ‘‘Calories’’ and the actual number of calories from § 101.36(e). J. Section 101.36 and Sample Labels Section 101.36(e)(11) shows two samples of Supplement Facts labels. The sample label in paragraph (e)(11)(ii) has an ingredient list that has ‘‘Sucrose’’ as the first ingredient. The correct term, however, is ‘‘sugar’’ instead of ‘‘sucrose,’’ so the technical PO 00000 Frm 00012 Fmt 4700 Sfmt 4700 amendment replaces ‘‘Sucrose’’ with ‘‘Sugar’’ in the sample label. The sample label in paragraph (e)(11)(iv) has an entry of 0 grams of trans fat. The technical amendment removes the trans fat line from the sample label because certain dietary ingredients or subcomponents, including trans fat, that are not present or are present in amounts that can be declared as zero, must not be declared on the Supplement Facts label (see § 101.36(b)(2)). The sample label in paragraph (e)(12) contained two errors. The sample label incorrectly placed choline after potassium when, under § 101.36(b)(2)(i)(B), choline should appear after pantothenic acid. Additionally, the sample label incorrectly gave a value for potassium. Under § 101.36(b)(2), vitamins and minerals cannot be declared on the Supplement Facts label that are not present, or that are present in amounts that can be declared as zero in § 101.9(c) (such as amounts corresponding to less than 2 percent of the RDI for the nutrient). In the sample label that appeared in the Nutrition Facts Label Final Rule, the level for potassium was less than 2 percent of the RDI. Consequently, the technical amendment revises the sample label to provide a level of potassium that would cause potassium to be listed on the Supplement Facts label. K. Appendix B and Examples of Graphic Enhancements Used by FDA The regulations at part 101 (21 CFR part 101) contain several appendices. One appendix, identified as Appendix B and entitled ‘‘Examples of Graphic Enhancements used by the FDA,’’ illustrates various features of the Nutrition Facts label and identifies type sizes, fonts, and other specifications that we use in our illustrations of the Nutrition Facts label. When we issued the Nutrition Facts Label Final Rule, we did not update Appendix B to correspond to the Nutrition Facts Label Final Rule’s new and revised requirements. The technical amendment, therefore, updates Appendix B so that the illustration corresponds to the Nutrition Facts Label Final Rule. The updated image also changes the value for potassium from 235 mg to 240 mg; the change to 240 mg is consistent with the rounding increments used for potassium when a serving contains greater than 140 mg of potassium. In such cases, the declared value is rounded to the nearest 10 mg increment. E:\FR\FM\21DER1.SGM 21DER1 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations III. The Administrative Procedure Act Publication of this document constitutes final action of these changes under the Administrative Procedure Act (APA) (5 U.S.C. 553). Under 5 U.S.C. 553(b)(3)(B) of the APA, an Agency may, for good cause, find (and incorporate the finding and a brief statement of reasons in the rules issued) that notice and public comment procedure on a rule is impracticable, unnecessary, or contrary to the public interest. We have determined that notice and public comment are unnecessary because these amendments only make technical or non-substantive changes, such as correcting sample labels, correcting cross-references, and restoring provisions that were never intended to be removed. For these reasons, we have determined that publishing a notice of proposed rulemaking and providing opportunity for public comment is unnecessary. In addition, FDA finds good cause for these amendments to become effective on the date of publication of this action. The APA allows an effective date less than 30 days after publication as provided by an Agency for good cause found and published with the rule (5 U.S.C. 553(d)(3)). A delayed effective date is unnecessary in this case because the amendments do not impose any new regulatory requirements on affected parties. As a result, affected parties do not need time to prepare before the rule takes effect. Therefore, we find good cause for this correction to become effective on the date of publication of this action. amozie on DSK3GDR082PROD with RULES IV. Paperwork Reduction Act of 1995 This final rule refers to previously approved collections of information found in FDA regulations. These collections of information are subject to review by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501– 3520). The collections of information in part 101 have been approved under OMB control number 0910–0381. V. Analysis of Environmental Impact We have determined under 21 CFR 25.30(h) that this action is of a type that does not individually or cumulatively have a significant effect on the human environment. Therefore, neither an environmental assessment nor an environmental impact statement is required. VI. Federalism We have analyzed this final rule in accordance with the principles set forth in Executive Order 13132. FDA has determined that the rule does not VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 contain policies that have substantial direct effects on the States, on the relationship between the National Government and the States, or on the distribution of power and responsibilities among the various levels of government. Accordingly, we conclude that the rule does not contain policies that have federalism implications as defined in the Executive order and, consequently, a federalism summary impact statement is not required. VII. Executive Order 13175: Consultation and Coordination With Indian Tribal Governments We have analyzed this rule in accordance with the principles set forth in Executive Order 13175. We have determined that the rule does not contain policies that have substantial direct effects on one or more Indian Tribes, on the relationship between the Federal Government and Indian Tribes, or on the distribution of power and responsibilities between the Federal Government and Indian Tribes. Accordingly, we conclude that the rule does not contain policies that have tribal implications as defined in the Executive Order and, consequently, a tribal summary impact statement is not required. List of Subjects in 21 CFR Part 101 Food labeling, Incorporation by reference, Nutrition, Reporting and recordkeeping requirements. Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs, 21 CFR part 101 is amended as follows: PART 101—FOOD LABELING 1. The authority citation for part 101 continues to read as follows: ■ Authority: 15 U.S.C. 1453, 1454, 1455; 21 U.S.C. 321, 331, 342, 343, 348, 371; 42 U.S.C. 243, 264, 271. 2. In § 101.9: a. Revise paragraph (b)(5)(vi); b. Add paragraphs (c)(2)(i) through (iv); ■ c. Revise paragraphs (c)(6)(i) introductory text, (c)(6)(iii), (c)(8)(ii) introductory text, (c)(8)(iv), (d)(1)(iii), (e)(5), and (e)(6)(i) and (ii); and ■ d. Add paragraphs (j)(13)(i)(A) and (B). The revisions and additions read as follows: ■ ■ ■ § 101.9 * Nutrition labeling of food. * * (b) * * * (5) * * * PO 00000 Frm 00013 * Fmt 4700 * Sfmt 4700 65497 (vi) Ounces with an appropriate visual unit of measure, as described in paragraph (b)(5)(iii) of this section, may be used for products that naturally vary in size as provided for in paragraph (b)(2)(i)(F) of this section. * * * * * (c) * * * (2) * * * (i) ‘‘Saturated fat,’’ or ‘‘Saturated’’: A statement of the number of grams of saturated fat in a serving defined as the sum of all fatty acids containing no double bonds, except that label declaration of saturated fat content information is not required for products that contain less than 0.5 gram of total fat in a serving if no claims are made about fat, fatty acid, or cholesterol content, and if ‘‘calories from saturated fat’’ is not declared. Except as provided for in paragraph (f) of this section, if a statement of the saturated fat content is not required and, as a result, not declared, the statement ‘‘Not a significant source of saturated fat’’ shall be placed at the bottom of the table of nutrient values. Saturated fat content shall be indented and expressed as grams per serving to the nearest 0.5 gram (1⁄2) gram increment below 5 grams and to the nearest gram increment above 5 grams. If the serving contains less than 0.5 gram, the content shall be expressed as zero. (ii) ‘‘Trans fat’’ or ‘‘Trans’’: A statement of the number of grams of trans fat in a serving, defined as the sum of all unsaturated fatty acids that contain one or more isolated (i.e., nonconjugated) double bonds in a trans configuration, except that label declaration of trans fat content information is not required for products that contain less than 0.5 gram of total fat in a serving if no claims are made about fat, fatty acid or cholesterol content. The word ‘‘trans’’ may be italicized to indicate its Latin origin. Trans fat content shall be indented and expressed as grams per serving to the nearest 0.5 (1⁄2)-gram increment below 5 grams and to the nearest gram increment above 5 grams. If the serving contains less than 0.5 gram, the content, when declared, shall be expressed as zero. Except as provided for in paragraph (f) of this section, if a statement of the trans fat content is not required and, as a result, not declared, the statement ‘‘Not a significant source of trans fat’’ shall be placed at the bottom of the table of nutrient values. (iii) ‘‘Polyunsaturated fat’’ or ‘‘Polyunsaturated’’ (VOLUNTARY): A statement of the number of grams of polyunsaturated fat in a serving defined as cis,cis-methylene-interrupted E:\FR\FM\21DER1.SGM 21DER1 amozie on DSK3GDR082PROD with RULES 65498 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations polyunsaturated fatty acids may be declared voluntarily, except that when monounsaturated fat is declared, or when a claim about fatty acids or cholesterol is made on the label or in labeling of a food other than one that meets the criteria in § 101.62(b)(1) for a claim for ‘‘fat free,’’ label declaration of polyunsaturated fat is required. Polyunsaturated fat content shall be indented and expressed as grams per serving to the nearest 0.5 (1⁄2) gram increment below 5 grams and to the nearest gram increment above 5 grams. If the serving contains less than 0.5 gram, the content shall be expressed as zero. (iv) ‘‘Monounsaturated fat’’ or ‘‘Monounsaturated’’ (VOLUNTARY): A statement of the number of grams of monounsaturated fat in a serving defined as cis-monounsaturated fatty acids may be declared voluntarily except that when polyunsaturated fat is declared, or when a claim about fatty acids or cholesterol is made on the label or in labeling of a food other than one that meets the criteria in § 101.62(b)(1) for a claim for ‘‘fat free,’’ label declaration of monounsaturated fat is required. Monounsaturated fat content shall be indented and expressed as grams per serving to the nearest 0.5 (1⁄2) gram increment below 5 grams and to the nearest gram increment above 5 grams. If the serving contains less than 0.5 gram, the content shall be expressed as zero. * * * * * (6) * * * (i) ‘‘Dietary fiber’’: A statement of the number of grams of total dietary fiber in a serving, indented and expressed to the nearest gram, except that if a serving contains less than 1 gram, declaration of dietary fiber is not required or, alternatively, the statement ‘‘Contains less than 1 gram’’ or ‘‘less than 1 gram’’ may be used, and if the serving contains less than 0.5 gram, the content may be expressed as zero. Dietary fiber is defined as non-digestible soluble and insoluble carbohydrates (with 3 or more monomeric units), and lignin that are intrinsic and intact in plants; isolated or synthetic non-digestible carbohydrates (with 3 or more monomeric units) determined by FDA to have physiological effects that are beneficial to human health. Except as provided for in paragraph (f) of this section, if dietary fiber content is not required, and as a result not declared, the statement ‘‘Not a significant source of dietary fiber’’ shall be placed at the bottom of the table of nutrient values in the same type size. The following isolated or synthetic nondigestible carbohydrate(s) have been VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 determined by FDA to have physiological effects that are beneficial to human health and, therefore, shall be included in the calculation of the amount of dietary fiber: [beta]-glucan soluble fiber (as described in § 101.81(c)(2)(ii)(A)), psyllium husk (as described in § 101.81(c)(2)(ii)(B)(1)), cellulose, guar gum, pectin, locust bean gum, and hydroxypropylmethylcellulose. The manufacturer must make and keep records in accordance with paragraphs (g)(10) and (11) of this section to verify the declared amount of dietary fiber in the label and labeling of food when a mixture of dietary fiber, and added nondigestible carbohydrate(s) that does not meet the definition of dietary fiber, is present in the food. * * * * * (iii) ‘‘Added Sugars’’: A statement of the number of grams of added sugars in a serving, except that label declaration of added sugars content is not required for products that contain less than 1 gram of added sugars in a serving if no claims are made about sweeteners, sugars, added sugars, or sugar alcohol content. Except as provided for in paragraph (f) of this section, if a statement of the added sugars content is not required and, as a result, not declared, the statement ‘‘Not a significant source of added sugars’’ shall be placed at the bottom of the table of nutrient values in the same type size. Added sugars are either added during the processing of foods, or are packaged as such, and include sugars (free, mono and disaccharides), sugars from syrups and honey, and sugars from concentrated fruit or vegetable juices that are in excess of what would be expected from the same volume of 100 percent fruit or vegetable juice of the same type, except that fruit or vegetable juice concentrated from 100 percent juices sold to consumers, fruit or vegetable juice concentrates used towards the total juice percentage label declaration under § 101.30 or for Brix standardization under § 102.33(g)(2) of this chapter, fruit juice concentrates which are used to formulate the fruit component of jellies, jams, or preserves in accordance with the standard of identities set forth in §§ 150.140 and 150.160 of this chapter, or the fruit component of fruit spreads shall not be labeled as added sugars. Added sugars content shall be indented under Total Sugars and shall be prefaced with the word ‘‘Includes’’ followed by the amount (in grams) ‘‘Added Sugars’’ (‘‘Includes ‘X’ g Added Sugars’’). It shall be expressed to the nearest gram, except that if a serving contains less than 1 PO 00000 Frm 00014 Fmt 4700 Sfmt 4700 gram, the statement ‘‘Contains less than 1 gram’’ or ‘‘less than 1 gram’’ may be used as an alternative, and if the serving contains less than 0.5 gram, the content may be expressed as zero. When a mixture of naturally occurring and added sugars is present in the food, and for specific foods containing added sugars, alone or in combination with naturally occurring sugars, where the added sugars are subject to fermentation and/or non-enzymatic browning, the manufacturer must make and keep records in accordance with paragraphs (g)(10) and (11) of this section to verify the declared amount of added sugars in the label and labeling of food. * * * * * (8) * * * (ii) The declaration of vitamins and minerals as a quantitative amount by weight and percent of the RDI shall include vitamin D, calcium, iron, and potassium in that order, for infants through 12 months, children 1 through 3 years of age, pregnant women, lactating women, and adults and children 4 or more years of age, except quantitative weights for these vitamins and minerals are not required for labels described in paragraph (j)(13) of this section. The declaration of folic acid shall be included as a quantitative amount by weight when added as a nutrient supplement or a claim is made about the nutrient. The declaration of vitamins and minerals in a food, as a quantitative amount by weight and percent of the RDI, may include any of the other vitamins and minerals listed in paragraph (c)(8)(iv) of this section. The declaration of vitamins and minerals shall include any of the other vitamins and minerals listed in paragraph (c)(8)(iv) of this section as a statement of the amount per serving of the vitamins and minerals as described in this paragraph (c)(8)(ii), calculated as a percent of the RDI and expressed as a percent of the Daily Value, when they are added as a nutrient supplement, or when a claim is made about them, unless otherwise stated as quantitative amount by weight and percent of the Daily Value. Other vitamins and minerals need not be declared if neither the nutrient nor the component is otherwise referred to on the label or the labeling or advertising and the vitamins and minerals are: * * * * * (iv) The following RDIs, nomenclature, and units of measure are established for the following vitamins and minerals which are essential in human nutrition: E:\FR\FM\21DER1.SGM 21DER1 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations 65499 RDI Adults and children ≥ 4 years Nutrient Unit of measure Vitamin D ....................... Calcium .......................... Iron ................................. Potassium ...................... Vitamin A ....................... Vitamin C ....................... Vitamin E ....................... Vitamin K ....................... Thiamin .......................... Riboflavin ....................... Niacin ............................. Vitamin B6 ...................... Folate 6 ........................... Vitamin B12 .................... Biotin .............................. Pantothenic acid ............ Phosphorus .................... Iodine ............................. Magnesium .................... Zinc ................................ Selenium ........................ Copper ........................... Manganese .................... Chromium ...................... Molybdenum .................. Chloride ......................... Choline ........................... Protein ........................... Micrograms (mcg) 2 ............................................. Milligrams (mg) .................................................... Milligrams (mg) .................................................... Milligrams (mg) .................................................... Micrograms RAE 3 (mcg) ..................................... Milligrams (mg) .................................................... Milligrams (mg) 4 .................................................. Micrograms (mcg) ................................................ Milligrams (mg) .................................................... Milligrams (mg) .................................................... Milligrams NE 5 (mg) ............................................ Milligrams (mg) .................................................... Micrograms DFE 7 (mcg) ..................................... Micrograms (mcg) ................................................ Micrograms (mcg) ................................................ Milligrams (mg) .................................................... Milligrams (mg) .................................................... Micrograms (mcg) ................................................ Milligrams (mg) .................................................... Milligrams (mg) .................................................... Micrograms (mcg) ................................................ Milligrams (mg) .................................................... Milligrams (mg) .................................................... Micrograms (mcg) ................................................ Micrograms (mcg) ................................................ Milligrams (mg) .................................................... Milligrams (mg) .................................................... Grams (g) ............................................................ Infants 1 through 12 months 20 1,300 18 4,700 900 90 15 120 1.2 1.3 16 1.7 400 2.4 30 5 1,250 150 420 11 55 0.9 2.3 35 45 2,300 550 N/A 10 260 11 700 500 50 5 2.5 0.3 0.4 4 0.3 80 0.5 6 1.8 275 130 75 3 20 0.2 0.6 5.5 3 570 150 11 Children 1 through 3 years 15 700 7 3,000 300 15 6 30 0.5 0.5 6 0.5 150 0.9 8 2 460 90 80 3 20 0.3 1.2 11 17 1,500 200 N/A Pregnant women and lactating women 15 1,300 27 5,100 1,300 120 19 90 1.4 1.6 18 2.0 600 2.8 35 7 1,250 290 400 13 70 1.3 2.6 45 50 2,300 550 8 71 1 RDIs are based on dietary reference intake recommendations for infants through 12 months of age. 2 The amount of vitamin D may, but is not required to, be expressed in international units (IU), in addition to the mandatory declaration in mcg. Any declaration of the amount of vitamin D in IU must appear in parentheses after the declaration of the amount of vitamin D in mcg. 3 RAE = Retinol activity equivalents; 1 microgram RAE = 1 microgram retinol, 2 microgram supplemental b-carotene, 12 micrograms dietary bcarotene, or 24 micrograms dietary a-carotene, or dietary 24 micrograms dietary b-cryptoxanthin. 4 1 mg a-tocopherol (label claim) = 1 mg a-tocopherol = 1 mg RRR- a-tocopherol = 2 mg all rac-a-tocopherol. 5 NE = Niacin equivalents, 1 mg NE = 1 mg niacin = 60 milligrams tryptophan. 6 ‘‘Folate’’ and ‘‘Folic Acid’’ must be used for purposes of declaration in the labeling of conventional foods and dietary supplements. The declaration for folate must be in mcg DFE (when expressed as a quantitative amount by weight in a conventional food or a dietary supplement), and percent DV based on folate in mcg DFE. Folate may be expressed as a percent DV in conventional foods. When folic acid is added or when a claim is made about the nutrient, folic acid must be declared in parentheses, as mcg of folic acid. 7 DFE = Dietary Folate Equivalents; 1 DFE = 1 mcg naturally occurring folate = 0.6 mcg folic acid. 8 Based on the reference caloric intake of 2,000 calories for adults and children aged 4 years and older, and for pregnant women and lactating women. * * * * (d)(1) * * * (iii) Information required in paragraphs (d)(7) and (8) of this section shall be in type size no smaller than 8 point. Information required in paragraph (d)(5) of this section for the ‘‘Calories’’ declaration shall be highlighted in bold or extra bold and shall be in a type size no smaller than 16 point except the type size for this information required in the tabular displays as shown in paragraphs (d)(11), (e)(6)(ii), and (j)(13)(ii)(A)(1) of this amozie on DSK3GDR082PROD with RULES * VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 section and the linear display for small packages as shown in paragraph (j)(13)(ii)(A)(2) of this section shall be in a type size no smaller than 10 point. The numeric amount for the information required in paragraph (d)(5) of this section shall also be highlighted in bold or extra bold type and shall be in a type size no smaller than 22 point, except the type size for this information required for the tabular display for small packages as shown in paragraph (j)(13)(ii)(A)(1) of this section, and for the linear display for small packages as PO 00000 Frm 00015 Fmt 4700 Sfmt 4700 shown in paragraph (j)(13)(ii)(A)(2) of this section no smaller than 14 point. The information required in paragraphs (d)(4), (6), and (9) of this section shall be in a type size no smaller than 6 point. When provided, the information described in paragraph (d)(10) of this section shall be in a type size no smaller than 6 point. * * * * * (e) * * * (5) The following sample label illustrates the provisions of paragraph (e) of this section: E:\FR\FM\21DER1.SGM 21DER1 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations amozie on DSK3GDR082PROD with RULES (6) * * * (i) Nutrient information for vitamins and minerals shall be separated from VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 information on other nutrients by a bar and shall be arrayed vertically in the following order: Vitamin D, calcium, PO 00000 Frm 00016 Fmt 4700 Sfmt 4700 iron, and potassium as shown in the following sample labels. E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.010</GPH> 65500 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations 65501 Dual Column Display, Per Serving and Per Container Nutrition Facts 2 servings per container Serving size 1 cup (255gJ Peraervlng Per container 220 440 Calories % DV* Total Fat Saturated Fat Trans Fat Cholesterol Sodium Total Carb. Dietary Fiber Total Sugars Incl. Added SUgars Protein 'li>DV" 13% 20% 5g 2g Og 15mg 240mg 35g 6g 7g 4g 9g 8% 10g 10% 4g Og 5% 30mg 10% 460mg 13% 70g 21% 12g 14g 8% Bg 18g 10% 21% 25% 43% Vitamin D 5mcg Calcium 200mg 1mg 470mg 25% 15% 6% 10% 50% 30% 10% 20% Iron Potassium 10mcg 400mg 2mg 940mg 18% • The % Dally Value (DV) tells you how much a nutrient In a serving of food contributes to a dally diet 2,000 calories a day Is used tor general VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 PO 00000 Frm 00017 Fmt 4700 Sfmt 4725 E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.011</GPH> amozie on DSK3GDR082PROD with RULES nutrition advice. Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations (b)(2)(i)(D) and (b)(12)(i) of this section for labels that use the tabular display. * nutrition information is provided, all required information shall be in type size no smaller than 6 point or all upper-case type of 1–16 inches minimum height, except that individual serving-size packages of food served with meals in restaurants, institutions, and on board passenger carriers, and not intended for sale at retail, may comply with § 101.2(c)(2). * * * * * * * * * (j) * * * (13)(i) * * * (A) The manufacturer, packer, or distributor shall provide on the label of packages that qualify for and use this exemption an address or telephone number that a consumer can use to obtain the required nutrition information (e.g., ‘‘For nutrition information, call 1–800–123–4567’’). (B) When such products bear nutrition labeling, either voluntarily or because nutrition claims or other VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 3. In § 101.36 revise paragraphs (b)(2)(i)(B) introductory text, ■ PO 00000 Frm 00018 Fmt 4700 Sfmt 4700 (b)(2)(ii)(B), (e) introductory text, (e)(11)(ii) and (iv), and (e)(12) to read as follows: § 101.36 Nutrition labeling of dietary supplements. * * * * * (b) * * * (2) * * * (i) * * * (B) The names of dietary ingredients that are declared under paragraph (b)(2)(i) of this section shall be presented in a column aligned on the E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.013</GPH> (ii) The following sample label illustrates the provisions of paragraphs ER21DE18.012</GPH> amozie on DSK3GDR082PROD with RULES 65502 left side of the nutritional label in the order and manner of indentation specified in § 101.9(c), except that calcium and iron shall follow choline, and sodium and potassium shall follow chloride. This results in the following order for vitamins and minerals: Vitamin A, vitamin C, vitamin D, vitamin E, vitamin K, thiamin, riboflavin, niacin, vitamin B6, folate and folic acid, vitamin B12, biotin, pantothenic acid, choline, calcium, iron, phosphorus, iodine, magnesium, zinc, selenium, copper, manganese, chromium, molybdenum, chloride, sodium, potassium, and fluoride. The (b)(2)-dietary ingredients shall be listed according to the nomenclature specified in § 101.9 or in paragraph (b)(2)(i)(B)(2) of this section. * * * * * (ii) * * * (B) The amounts of vitamins and minerals, excluding sodium, shall be the amount of the vitamin or mineral included in one serving of the product, using the units of measurement and the levels of significance given in § 101.9(c)(8)(iv), except that zeros following decimal points may be dropped, and additional levels of significance may be used when the number of decimal places indicated is not sufficient to express lower amounts (e.g., the RDI for zinc is given in whole milligrams (mg), but the quantitative amount may be declared in tenths of a mg). The amount of vitamin D may, but is not required to, be expressed in IUs, in addition to the mandatory declaration in mcg. Any declaration of the amount of vitamin D in IUs must appear in * (iv) Dietary supplement containing dietary ingredients with and without RDIs and DRVs: * * VerDate Sep<11>2014 * * 16:23 Dec 20, 2018 Jkt 247001 PO 00000 Frm 00019 Fmt 4700 Sfmt 4700 65503 parentheses after the declaration of the amount of vitamin D in mcg. * * * * * (e) Except as provided for small and intermediate sized packages under paragraph (h)(3)(i)(2) of this section, information other than the title, headings, and footnotes shall be in uniform type size no smaller than 8 point. Type size no smaller than 6 point may be used for column headings (e.g., ‘‘Amount Per Serving’’ and ‘‘% Daily Value’’) and for footnotes (e.g., ‘‘Percent Daily Values are based on a 2,000 calorie diet’’). * * * * * (11) * * * (ii) Multiple vitamins for children and adults (excludes Servings Per Container which is stated in the net quantity of contents declaration): E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.014</GPH> amozie on DSK3GDR082PROD with RULES Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations 65504 Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations * * * * (12) If space is not adequate to list the required information as shown in the sample labels in paragraph (e)(11) of this section, the list may be split and continued to the right as long as the headings are repeated. The list to the right must be set off by a line that distinguishes it and sets it apart from the dietary ingredients and percent of Daily Value information given to the left. The following sample label illustrates this display: * ■ 4. Revise appendix B to part 101 to read as follows: Appendix B to Part 101—Graphic Enhancements Used by the FDA * * * ER21DE18.016</GPH> * VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 PO 00000 Frm 00020 Fmt 4700 Sfmt 4700 E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.015</GPH> amozie on DSK3GDR082PROD with RULES * Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations 65505 Examples ofGrapble Enbaneenwtts used by the FDA 1. The Nutrition Facts label is boxed and contains all black or one oolortype printed on a white or neutral background. B. Typeteee and me 1. The "Nutrition Facts"label uses 6 point or larger Helvetica Black and/or Helvetica Regular type. In order to fit some formats, the typography may be kemed as much as 4 (tighter kerning reduces legibility). 2. Key nutrients and their% DailyValuesare set in 8 point Helvetica Black. The"%" symbol also may be set in Helvetica Black. 3...Nutrition Facts" is set in either Franklin Gothic Heavy or Helvetica Black to fit the width of the lab'et flush left 1llld tlU$hright 4. "Servings per container" is set in 10 point Helvetica Regular and "Serving size" is set in 10 point Helvetica Black and with 1 point ot leading. ''Amount per serving'' is set in 6 point Helvetica Black. 5. "Calories"' is set in 16 .point Helvetiea Black and the numerical value of calories is set in 22. point Helvetica Black. 6. Absolute measures of nutrient content (for exampt~. ''l g'') .and .nutrient subgroups are set in a point Helvetica Regular with.4 points of leading, 7. Vitamins and minerals are set in 8 point Helvetica Regular, with 4 points of leading, separated by 8 point bullets. 8. The type for the footnote is set in 6 point Helvetica Regular with 1 point ofleading. C. Rules 1. A 7 point rule separates large groupings as shown in the example. A 3 point rule separates calorie information from the nutrient infonnation. 2. A hairline rule or !4 point rule separates individual nutrients, as shown in the example. Descendeta do not touch rule. The top half of the label (nutrient infonnati.on) has 2 points of leading between the type and the rules and the bottom half ofthe label (footnote) has 1 point of leading between the type and the rules. The rule above the ..Added Sugars~• declaration is shortened as shown in the example. D. Box VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 PO 00000 Frm 00021 Fmt 4700 Sfmt 4725 E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.017</GPH> amozie on DSK3GDR082PROD with RULES 1. All labels are enclOsed by* point box rule within 3 points oftext m.easure. Federal Register / Vol. 83, No. 245 / Friday, December 21, 2018 / Rules and Regulations Dated: December 13, 2018. Scott Gottlieb, Commissioner of Food and Drugs. DEPARTMENT OF THE INTERIOR standards and to make other minor edits and additions for clarity. DATES: Effective Date: January 22, 2019. FOR FURTHER INFORMATION CONTACT: Jennifer Lawson at (202) 632–7003 or by fax (202) 632–7066 (these numbers are not toll free). SUPPLEMENTARY INFORMATION: National Indian Gaming Commission I. Background [FR Doc. 2018–27431 Filed 12–19–18; 8:45 am] BILLING CODE 4164–01–P 25 CFR Part 543 RIN 3141–AA60 Minimum Internal Control Standards National Indian Gaming Commission, Interior. ACTION: Final rule. amozie on DSK3GDR082PROD with RULES AGENCY: The National Indian Gaming Commission (NIGC) amends its minimum internal control standards for Class II gaming under the Indian Gaming Regulatory Act to correct an erroneous deletion of the key control SUMMARY: VerDate Sep<11>2014 16:23 Dec 20, 2018 Jkt 247001 The Indian Gaming Regulatory Act (IGRA or Act), Public Law 100–497, 25 U.S.C. 2701 et seq., was signed into law on October 17, 1988. The Act established the National Indian Gaming Commission (‘‘NIGC’’ or ‘‘Commission’’) and set out a comprehensive framework for the regulation of gaming on Indian lands. On January 5, 1999, the NIGC published a final rule in the Federal Register called Minimum Internal Control Standards. 64 FR 590. The rule added a new part to the Commission’s regulations establishing Minimum Internal Control Standards (MICS) to reduce the risk of loss because of PO 00000 Frm 00022 Fmt 4700 Sfmt 4700 customer or employee access to cash and cash equivalents within a casino. The rule contains standards and procedures that govern cash handling, documentation, game integrity, auditing, surveillance, and variances, as well as other areas. The Commission recognized from their inception that the MICS would require periodic review and updates to keep pace with technology and has substantively amended them numerous times, most recently in late 2013 (78 FR 63873). II. Development of the Rule On September 21, 2012, the Commission concluded nearly two years of consultation and drafting with the publication of comprehensive amendments, additions, and updates to Part 543, the minimum internal control standards (MICS) for Class II gaming operations (77 FR 58708). The regulations require tribes to establish controls and implement procedures at least as stringent as those described in E:\FR\FM\21DER1.SGM 21DER1 ER21DE18.018</GPH> 65506

Agencies

[Federal Register Volume 83, Number 245 (Friday, December 21, 2018)]
[Rules and Regulations]
[Pages 65493-65506]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-27431]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 101

[Docket No. FDA-2012-N-1210]


Food Labeling; Revision of the Nutrition and Supplement Facts 
Labels; Technical Amendments

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; technical amendment.

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SUMMARY: The Food and Drug Administration (FDA or we) is amending the 
regulations pertaining to the Nutrition Facts and Supplement Facts 
labels. The amendments correct errors that were made in labeling 
examples, restore incorrect deletions, correct the edition of a 
reference cited in the rule, and correct cross-references to other 
regulations. This action is ministerial or editorial in nature.

DATES: This rule is effective December 21, 2018.

FOR FURTHER INFORMATION CONTACT: Mark Kantor, Center for Food Safety 
and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., 
College Park, MD 20740, 240-402-2082.

SUPPLEMENTARY INFORMATION:

I. Background

    In the Federal Register of May 27, 2016 (81 FR 33742 and 81 FR 
34000), we published two final rules entitled ``Food Labeling: Revision 
of the Nutrition and Supplement Facts Labels'' (the Nutrition Facts 
Label Final Rule) and ``Food Labeling: Serving Sizes of Foods That Can 
Reasonably Be Consumed At One Eating Occasion; Dual-Column Labeling; 
Updating, Modifying, and Establishing Certain Reference Amounts 
Customarily Consumed; Serving Size for Breath Mints; and Technical 
Amendments'' (the Serving Size Final Rule). The Nutrition Facts Label 
Final Rule revises the Nutrition Facts label by:

     Removing the declaration of ``Calories from fat'' 
because current science supports a view that the type of fat is more 
relevant than overall total fat intake in increased risk of chronic 
diseases;

[[Page 65494]]

     requiring the declaration of the gram amount of ``added 
sugars'' in a serving of a product, establishing a Daily Reference 
Value (DRV), and requiring the percent Daily Value (DV) declaration 
for added sugars;
     changing ``Sugars'' to ``Total Sugars'' and requiring 
that ``Includes `X' g Added Sugars'' be indented and declared 
directly below ``Total Sugars'' on the label;
     updating the list of vitamins and minerals of public 
health significance. For example, the Nutrition Facts Label Final 
Rule requires the declaration of vitamin D and potassium and 
permits, rather than requires, the declaration of vitamins A and C;
     updating certain reference values used in the 
declaration of percent DVs of nutrients on the Nutrition Facts and 
Supplement Facts labels;
     revising the format of the Nutrition Facts label to 
increase the prominence of the term ``Calories;''
     removing the requirement for the footnote table listing 
the reference values for certain nutrients for 2,000 and 2,500 
calorie diets;
     requiring the maintenance of records to support the 
declarations of certain nutrients under specified circumstances. For 
example, because there are no analytical methods that can 
distinguish between dietary fiber (soluble and insoluble fiber) and 
nondigestible carbohydrates that do not meet the definition of 
dietary fiber; added and naturally occurring sugars or the various 
forms of vitamin E; or folate and folic acid, the Nutrition Facts 
Label Final Rule requires manufacturers to make and keep certain 
written records to verify the declarations of dietary fiber, added 
sugars, vitamin E, and folate and folic acid in the labeling of the 
food associated with such records. The Nutrition Facts Label Final 
Rule requires these records to be kept for at least 2 years after 
introduction or delivery for introduction of the food into 
interstate commerce. A similar requirement exists with respect to 
added sugars in foods subject to nonenzymatic browning and 
fermentation because there are no analytical methods that can 
determine the amount of added sugar in specific foods containing 
added sugars alone or in combination with naturally occurring 
sugars, where the added sugars are subject to nonenzymatic browning 
and fermentation. However, for manufacturers of such foods who are 
unable to reasonably approximate the amount of added sugars in a 
serving of food to which the records requirements apply, the 
Nutrition Facts Label Final Rule allows manufacturers to submit a 
petition to request an alternative means of compliance; and
     establishing a compliance date of 2 years after the 
Nutrition Facts Label Final Rule's effective date, except that 
manufacturers with less than $10 million in annual food sales have a 
compliance date of 3 years after the Nutrition Facts Label Final 
Rule's effective date. (In the Federal Register of May 4, 2018 (83 
FR 19619), however, we extended the compliance date for 
manufacturers with $10 million or more in annual food sales from 
July 26, 2018, to January 1, 2020, and the compliance date for 
manufacturers with less than $10 million in annual food sales from 
July 26, 2019, to January 1, 2021.)
    The Serving Size Final Rule requires all containers, including 
containers of products with ``large'' reference amounts customarily 
consumed (RACCs) (i.e., products with RACCs of at least 100 grams 
(g) or 100 milliliters (mL)), containing less than 200 percent of 
the RACC to be labeled as a single-serving container. Except for 
when certain exceptions apply, the Serving Size Final Rule further 
requires that containers and units that contain at least 200 percent 
and up to and including 300 percent of the RACC be labeled with a 
column of nutrition information within the Nutrition Facts label 
that lists the quantitative amounts and percent DVs for the entire 
container, in addition to the required column listing the 
quantitative amounts and percent DVs for a serving that is less than 
the entire container (i.e., the serving size derived from the RACC). 
The Serving Size Final Rule also updates, modifies, and establishes 
RACCs for certain foods and product categories.

II. Description of the Technical Amendments

    Since we published the two final rules in the Federal Register, we 
have noted or have been made aware of errors that appeared in the final 
rules. Most errors are non-substantive; for example, Sec.  101.9(e)(5) 
and (6) (21 CFR 101.9(e)(5) and (6)) show sample Nutrition Facts 
labels. The sample labels, however, differed from the other sample 
labels in the Nutrition Facts Label Final Rule in that the line 
underneath ``Saturated Fat'' did not extend completely to the left edge 
of the label. Through this technical amendment, we are revising the 
sample labels so that the line extends completely to the left edge of 
the label.
    Other errors reflected inconsistencies between the Nutrition Facts 
Label Final Rule's requirements and sample labels. For example, one 
sample label omitted information regarding the number of servings per 
container and serving size; both information elements are required. 
Through this technical amendment, we are revising the sample label to 
include the missing information.
    Three errors resulted in the removal of preexisting provisions even 
though the Nutrition Facts Label Final Rule did not intend to remove 
those provisions. To the contrary, the preamble to the Nutrition Facts 
Label Final Rule discussed the provisions as still existing. 
Consequently, the technical amendment restores those provisions.
    Other errors pertained to cross-references; in some instances, the 
Nutrition Facts Label Final Rule and the Serving Size Final Rule 
mistakenly referred to a different provision. In another instance, the 
Nutrition Facts Label Final Rule omitted a cross-reference to another 
provision. The technical amendment corrects the cross-references.
    We describe the amendments in more detail below.

A. Section 101.9(b) and a Cross-Reference

    Section 101.9(b)(2)(i) provides, in part, the requirements for 
serving sizes for products in discrete units (e.g., muffins, sliced 
products, such as sliced bread, or individually packaged products 
within a multiserving package). The Serving Size Final Rule revised 
Sec.  101.9(b)(2)(i) by removing paragraph (b)(2)(i)(E) (which had 
pertained to the serving size declaration of individual units in 
certain multiserving packages where the product has a reference amount 
of 100 grams (or milliliters) or larger) and redesignated paragraphs 
(b)(2)(i)(F) through (I) accordingly (see 81 FR 34000 at 34040). For 
example, Sec.  101.9(b)(2)(i)(G) was redesignated as Sec.  
101.9(b)(2)(i)(F).
    However, the Serving Size Final Rule neglected to revise a 
reference to previous Sec.  101.9(b)(2)(i)(G) that appears in Sec.  
101.9(b)(5)(vi) (which pertains to ounces as a common household 
measure, with an appropriate visual unit of measure, for products that 
naturally vary in size). Consequently, we are revising Sec.  
101.9(b)(5)(vi) to refer to Sec.  101.9(b)(2)(i)(F).

B. Section 101.9(c)(2) and Statements Regarding Saturated Fat, Trans 
Fat, Polyunsaturated Fat, and Monounsaturated Fat

    Section 101.9(c)(2) discusses how a statement of the number of 
grams of total fat in a serving must be expressed. Before we issued the 
Nutrition Facts Label Final Rule, Sec.  101.9(c)(2) contained four 
subordinate paragraphs that discussed how the number of grams of 
saturated fat, trans fat, polyunsaturated fat, and monounsaturated fat 
must be expressed; these subordinate paragraphs were numbered as Sec.  
101.9(c)(2)(i) through (iv). The Nutrition Facts Label Final Rule did 
not amend or revise these subordinate paragraphs; to the contrary, in 
the preamble to the Nutrition Facts Label Final Rule, we either 
referred to them to describe an existing requirement or expressly 
stated that we did not intend to change them (see 81 FR 33742 at 33785, 
33860).
    Nevertheless, after we published the Nutrition Facts Label Final 
Rule, we learned that Sec.  101.9(c)(2)(i) through (iv) had been 
removed from the Code of Federal Regulations. Because we did not intend 
such a result, the technical amendment restores Sec.  101.9(c)(2)(i) 
through (iv).

[[Page 65495]]

C. Section 101.9(c)(6)(i), Fiber, and a Cross-Reference

    Section 101.9(c)(6)(i) discusses, among other things, specific 
isolated or synthetic non-digestible carbohydrates that we have 
determined to have physiological effects that are beneficial to human 
health and that must be included in the calculation of the amount of 
dietary fiber. One such carbohydrate is psyllium husk, and the 
Nutrition Facts Label Final Rule contained a cross-reference to Sec.  
101.81(c)(2)(ii)(A)(6) (21 CFR 101.81(c)(2)(ii)(A)(6)).
    The cross-reference was in error. The correct cross-reference is 
Sec.  101.81(c)(2)(ii)(B)(1), and so we have revised Sec.  
101.9(c)(6)(i) accordingly.

D. Section 101.9(c)(6)(iii), Added Sugars, and Simplified Format

    Section 101.9(c)(6)(iii) discusses how the ``added sugars'' 
statement must appear. The provision states, among other things, that 
if a statement of the added sugars content is not required and, as a 
result, is not declared on the Nutrition Facts label, then the 
statement ``Not a significant source of added sugars'' must be placed 
at the bottom of the table of nutrient values.
    However, Sec.  101.9(f) discusses when the declaration of nutrition 
information may be presented in a simplified format. In general, a 
simplified format may be used when a food product contains 
insignificant amounts of eight or more of specific nutrients; these 
nutrients include ``added sugars.'' Therefore, the technical amendment 
revises Sec.  101.9(c)(6)(iii) by adding ``Except as provided for in 
paragraph (f) of this section,'' at the start of the sentence 
describing where the statement, ``Not a significant source of added 
sugars,'' must be placed.

E. Section 101.9(c)(8)(ii) and Quantitative Weight and Sec.  
101.9(c)(8)(iv) and Retinol Activity Equivalents (RAE) and the Order of 
Nutrients on the Nutrition Facts Label

    Section 101.9(c)(8) establishes requirements related to the 
disclosure of vitamins and minerals on the Nutrition Facts label. The 
rule, at Sec.  101.9(c)(8)(ii), discusses the declaration of vitamins 
and minerals as a quantitative amount by weight and percent of the 
Reference Daily Intake (RDI). In the preamble to the proposed rule to 
revise the Nutrition Facts and Supplement Facts labels, we described 
the proposed rule as requiring the declaration of the absolute amounts 
for all mandatory and voluntary vitamins and minerals, in addition to 
the requirement for percent DV declaration; we also said that an 
exception to the proposed requirement would be Nutrition Facts labels 
for foods in small packages that have a total surface area available to 
bear labeling of 40 or less square inches (79 FR 11880 at 11952, March 
3, 2014). The preamble to the Nutrition Facts Label Final Rule noted 
the same exception for smaller packages (81 FR 33742 at 33946).
    However, the codified text inadvertently omitted the language 
creating the exception. Consequently, we are restoring the exception to 
Sec.  101.9(c)(8)(ii) so that the declaration of quantitative weights 
for these vitamins and minerals are not required for labels described 
in Sec.  101.9(j)(13).
    Additionally, Sec.  101.9(c)(8)(ii) contains a sentence mentioning 
the statement of the amount per serving of the vitamins and minerals 
``as described in this paragraph.'' To clarify the reference of ``this 
paragraph,'' the technical amendment revises ``this paragraph'' to read 
as ``this paragraph (c)(8)(ii)''.
    Our regulations, at Sec.  101.9(c)(8)(iv), describe, among other 
things, the units of measure for certain vitamins and minerals. The 
rule lists the nutrients, their units of measure, and their RDIs in a 
table; for vitamin A, the unit of measure is in micrograms RAE. 
Footnote 2 to the table explains that RAE means retinol activity 
equivalents and that 1 microgram RAE equals 1 microgram retinol, 2 
microgram supplemental [beta]-carotene, 12 micrograms [beta]-carotene, 
or 24 micrograms [alpha]-carotene, or 24 micrograms [beta]-
cryptoxanthin.
    In the preamble to the Nutrition Facts Label Final Rule, in 
response to a comment regarding the unit of measure for vitamin A, we 
explained that the conversions for microgram RAE were 1 retinol 
activity equivalent (mcg RAE) = 1 mcg retinol, 2 mcg supplemental 
[beta]-carotene, 12 mcg of dietary [beta]-carotene, or 24 mcg of other 
dietary provitamin A carotenoids ([alpha]-carotene or [beta]-
cryptoxanthin) (81 FR 33742 at 33913) (emphasis added). However, we 
neglected to insert the word ``dietary'' before [beta]-carotene, 
[alpha]-carotene, and [beta]-cryptoxanthin in footnote 2.
    The technical amendment inserts ``dietary'' before [beta]-carotene, 
[alpha]-carotene, and [beta]-cryptoxanthin in the footnote and also 
renumbers the footnote as footnote 3. The renumbering of the footnote 
is necessary because the technical amendment also revises the order of 
the nutrients in the table at 21 CFR 101.8(c)(8)(iv); the nutrients 
were supposed to be placed in order so that nutrients that must be 
disclosed on the label appear first. However, the Nutrition Facts Label 
Final Rule inadvertently neglected to reorder the nutrients in the 
table to reflect the status of vitamin D, calcium, iron, and potassium 
as nutrients that must be disclosed. As a result of reordering the 
nutrients in the table, footnote 2 is now footnote 3.

F. Section 101.9(d)(1)(iii) and Type Size

    Section 101.9(d)(1)(iii) establishes the type sizes for information 
on the Nutrition Facts label. Among other things, the regulation 
requires information required under Sec.  101.9(d)(9) (regarding the 
footnote to the Nutrition Facts label) to be in a type size no smaller 
than 6 point.
    In the preamble to the Nutrition Facts Label Final Rule, we 
discussed how other information pertaining to ``Amount per serving'' 
and ``% Daily Value'' also would be required to be in a type size no 
smaller than 6 point (see 81 FR 33742 at 33944 (discussing the type 
size for ``Amount per serving'') and 81 FR 33742 at 33952 (discussing 
the type size for ``% Daily Value'')). However, the codified text at 
Sec.  101.9(d)(1)(iii) omitted the paragraph designations for ``Amount 
per serving'' and ``% Daily Value,'' which are Sec.  101.9(d)(4) and 
(6), respectively. Consequently, the technical amendment adds 
paragraphs (d)(4) and (6) to the information that must be in a type 
size no smaller than 6 point.

G. Section 101.9(e)(5) and (6) and Corrections to Sample Labels

    Section 101.9(e)(5) and (6) show sample Nutrition Facts labels. The 
sample labels illustrate how dual column labels might appear. Some 
sample labels, however, differed from the other sample labels in the 
Nutrition Facts Label Final Rule in that the line underneath 
``Saturated Fat'' did not extend completely to the left edge of the 
label.
    The technical amendment revises the sample labels so that the line 
extends completely to the left edge of the label.
    In Sec.  101.9(e)(5), the revised sample label also changes the 
value for potassium from 45 mg to 40 mg because the declaration of 
potassium is to be expressed to the nearest 10 mg. increment.
    Additionally, in Sec.  101.9(e)(6)(i), we have revised the title 
for one sample label from ``Dual Column Display'' to ``Dual Column 
Display, Per Serving and Per Container.'' This revised title should 
help distinguish this sample label from the other sample label in Sec.  
101.9(e)(6)(i). As for the other sample label titled ``Dual Columns, 
Per Serving and Per Unit''), the sample label inadvertently omitted 
information regarding the

[[Page 65496]]

servings per container and serving size. The technical amendment 
revises the sample label for ``Dual Columns, Per Serving and Per Unit'' 
to include information on servings per container and serving size.
    In Sec.  101.9(e)(6)(ii), the sample label appeared blurred or 
difficult to read when printed in the Federal Register.
    The technical amendment substitutes a better quality image for the 
sample label. There are no changes to the contents of the sample label 
itself.

H. Section 101.9(j)(13) and Addresses or Phone Numbers for Obtaining 
Required Nutrition Information and the Exception for Certain Individual 
Serving Size Packages

    Section 101.9(j)(13)(i) discusses requirements for foods in small 
packages. The Nutrition Facts Label Final Rule revised Sec.  
101.9(j)(13)(i) so that the Nutrition Facts label on small packages 
would not be required to bear a footnote explaining what the ``% Daily 
Value'' means and manufacturers could voluntarily include an 
abbreviated footnote of ``% DV = % Daily Value'' in a type size no 
smaller than 6 point.
    In revising Sec.  101.9(j)(13)(i), we did not intend to affect the 
preexisting paragraphs at Sec.  101.9(j)(13)(i)(A), which pertains to 
the use of an address or telephone number where consumers can obtain 
required information, and Sec.  101.9(j)(13)(i)(B), which pertains to 
an exception for certain individual serving size packages of food. 
After we issued the Nutrition Facts Label Final Rule, we were informed 
that both paragraphs (j)(13)(i)(A) and (B) had, nevertheless, been 
deleted. Because we did not intend such a result, we are restoring 
paragraphs (j)(13)(i)(A) and (B) to Sec.  101.9(j)(13)(i) and also 
correcting an error in Sec.  101.9(j)(13)(i)(B) by replacing the 
reference to ``Sec.  101.2(c)(5)'' with ``Sec.  101.2(c)(2).'' The 
correction is necessary because Sec.  101.2(c)(5) does not exist, and 
the correct reference is to Sec.  101.2(c)(2).

I. Section 101.36 and Corrections to the Spelling of Phosphorus, the 
Listing of Potassium, the Size of Calories, and a Cross-Reference

    Section 101.36(b)(2)(i)(B) (21 CFR 101.36(b)(2)(i)(B)) names 
dietary ingredients that are to be declared on the Supplement Facts 
label. The Nutrition Facts Label Final Rule incorrectly spelled 
phosphorus as ``phosphorous,'' so the technical amendment uses the 
correct spelling. Additionally, we have replaced ``Vitamin A'' with 
``vitamin A'' for purposes of punctuation.
    Section 101.36(b)(2)(ii)(B) discusses how the amounts of vitamins 
and minerals must be declared on the Supplement Facts label. In brief, 
the regulation states that the amounts of vitamins and minerals, 
excluding sodium and potassium, must be the amount of vitamin or 
mineral included in one serving of the product, using the units of 
measurement and levels of significance given in Sec.  101.9(c)(8)(iv). 
The exclusion regarding potassium was based originally on the fact that 
there was no RDI value for potassium. The technical amendment deletes 
``and potassium'' from the exclusion in Sec.  101.36(b)(2)(ii)(B) 
because Sec.  101.9(c)(8)(iv), among other things, does set forth the 
RDI, nomenclature, and unit of measure for potassium. Thus, because 
Sec.  101.9(c)(8)(iv) sets forth an RDI and units of measure for 
potassium, the exclusion for potassium in Sec.  101.36(b)(2)(ii)(B) is 
no longer appropriate.
    Section 101.36(e) discusses type sizes for certain information on 
the Supplement Facts label. The rule specifies a minimum type size for 
footnotes (among other things) and gives an example of a footnote 
statement. However, the example, ``Percent Daily Values are based on a 
2,000 calorie diet,'' was missing a quotation mark. The technical 
amendment restores the missing quotation mark for the phrase ``Percent 
Daily Values are based on a 2,000 calorie diet.''
    Additionally, Sec.  101.36(e) contains a sentence specifying the 
font size for ``Calories'' and the heading ``Calories'' and the actual 
number of calories per serving. This sentence, however, should have 
been removed from the codified text because, as we stated in our 
response to comment 483 in the Nutrition Facts Label Final Rule, many 
dietary supplement products may contribute a negligible amount of 
calories (81 FR 33742 at 33939). We stated that the Nutrition Facts 
Label Final Rule does not require information about calories to be 
displayed in a larger type size or highlighted on any Supplement Facts 
labels (id.). Therefore, we are removing the sentence regarding the 
font size and highlighting for ``Calories'' and the actual number of 
calories from Sec.  101.36(e).

J. Section 101.36 and Sample Labels

    Section 101.36(e)(11) shows two samples of Supplement Facts labels. 
The sample label in paragraph (e)(11)(ii) has an ingredient list that 
has ``Sucrose'' as the first ingredient.
    The correct term, however, is ``sugar'' instead of ``sucrose,'' so 
the technical amendment replaces ``Sucrose'' with ``Sugar'' in the 
sample label.
    The sample label in paragraph (e)(11)(iv) has an entry of 0 grams 
of trans fat.
    The technical amendment removes the trans fat line from the sample 
label because certain dietary ingredients or subcomponents, including 
trans fat, that are not present or are present in amounts that can be 
declared as zero, must not be declared on the Supplement Facts label 
(see Sec.  101.36(b)(2)).
    The sample label in paragraph (e)(12) contained two errors. The 
sample label incorrectly placed choline after potassium when, under 
Sec.  101.36(b)(2)(i)(B), choline should appear after pantothenic acid. 
Additionally, the sample label incorrectly gave a value for potassium. 
Under Sec.  101.36(b)(2), vitamins and minerals cannot be declared on 
the Supplement Facts label that are not present, or that are present in 
amounts that can be declared as zero in Sec.  101.9(c) (such as amounts 
corresponding to less than 2 percent of the RDI for the nutrient). In 
the sample label that appeared in the Nutrition Facts Label Final Rule, 
the level for potassium was less than 2 percent of the RDI. 
Consequently, the technical amendment revises the sample label to 
provide a level of potassium that would cause potassium to be listed on 
the Supplement Facts label.

K. Appendix B and Examples of Graphic Enhancements Used by FDA

    The regulations at part 101 (21 CFR part 101) contain several 
appendices. One appendix, identified as Appendix B and entitled 
``Examples of Graphic Enhancements used by the FDA,'' illustrates 
various features of the Nutrition Facts label and identifies type 
sizes, fonts, and other specifications that we use in our illustrations 
of the Nutrition Facts label.
    When we issued the Nutrition Facts Label Final Rule, we did not 
update Appendix B to correspond to the Nutrition Facts Label Final 
Rule's new and revised requirements. The technical amendment, 
therefore, updates Appendix B so that the illustration corresponds to 
the Nutrition Facts Label Final Rule. The updated image also changes 
the value for potassium from 235 mg to 240 mg; the change to 240 mg is 
consistent with the rounding increments used for potassium when a 
serving contains greater than 140 mg of potassium. In such cases, the 
declared value is rounded to the nearest 10 mg increment.

[[Page 65497]]

III. The Administrative Procedure Act

    Publication of this document constitutes final action of these 
changes under the Administrative Procedure Act (APA) (5 U.S.C. 553). 
Under 5 U.S.C. 553(b)(3)(B) of the APA, an Agency may, for good cause, 
find (and incorporate the finding and a brief statement of reasons in 
the rules issued) that notice and public comment procedure on a rule is 
impracticable, unnecessary, or contrary to the public interest. We have 
determined that notice and public comment are unnecessary because these 
amendments only make technical or non-substantive changes, such as 
correcting sample labels, correcting cross-references, and restoring 
provisions that were never intended to be removed. For these reasons, 
we have determined that publishing a notice of proposed rulemaking and 
providing opportunity for public comment is unnecessary.
    In addition, FDA finds good cause for these amendments to become 
effective on the date of publication of this action. The APA allows an 
effective date less than 30 days after publication as provided by an 
Agency for good cause found and published with the rule (5 U.S.C. 
553(d)(3)). A delayed effective date is unnecessary in this case 
because the amendments do not impose any new regulatory requirements on 
affected parties. As a result, affected parties do not need time to 
prepare before the rule takes effect. Therefore, we find good cause for 
this correction to become effective on the date of publication of this 
action.

IV. Paperwork Reduction Act of 1995

    This final rule refers to previously approved collections of 
information found in FDA regulations. These collections of information 
are subject to review by the Office of Management and Budget (OMB) 
under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520). The 
collections of information in part 101 have been approved under OMB 
control number 0910-0381.

V. Analysis of Environmental Impact

    We have determined under 21 CFR 25.30(h) that this action is of a 
type that does not individually or cumulatively have a significant 
effect on the human environment. Therefore, neither an environmental 
assessment nor an environmental impact statement is required.

VI. Federalism

    We have analyzed this final rule in accordance with the principles 
set forth in Executive Order 13132. FDA has determined that the rule 
does not contain policies that have substantial direct effects on the 
States, on the relationship between the National Government and the 
States, or on the distribution of power and responsibilities among the 
various levels of government. Accordingly, we conclude that the rule 
does not contain policies that have federalism implications as defined 
in the Executive order and, consequently, a federalism summary impact 
statement is not required.

VII. Executive Order 13175: Consultation and Coordination With Indian 
Tribal Governments

    We have analyzed this rule in accordance with the principles set 
forth in Executive Order 13175. We have determined that the rule does 
not contain policies that have substantial direct effects on one or 
more Indian Tribes, on the relationship between the Federal Government 
and Indian Tribes, or on the distribution of power and responsibilities 
between the Federal Government and Indian Tribes. Accordingly, we 
conclude that the rule does not contain policies that have tribal 
implications as defined in the Executive Order and, consequently, a 
tribal summary impact statement is not required.

List of Subjects in 21 CFR Part 101

    Food labeling, Incorporation by reference, Nutrition, Reporting and 
recordkeeping requirements.

    Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
authority delegated to the Commissioner of Food and Drugs, 21 CFR part 
101 is amended as follows:

PART 101--FOOD LABELING

0
1. The authority citation for part 101 continues to read as follows:

    Authority:  15 U.S.C. 1453, 1454, 1455; 21 U.S.C. 321, 331, 342, 
343, 348, 371; 42 U.S.C. 243, 264, 271.

0
2. In Sec.  101.9:
0
a. Revise paragraph (b)(5)(vi);
0
b. Add paragraphs (c)(2)(i) through (iv);
0
c. Revise paragraphs (c)(6)(i) introductory text, (c)(6)(iii), 
(c)(8)(ii) introductory text, (c)(8)(iv), (d)(1)(iii), (e)(5), and 
(e)(6)(i) and (ii); and
0
d. Add paragraphs (j)(13)(i)(A) and (B).
    The revisions and additions read as follows:


Sec.  101.9  Nutrition labeling of food.

* * * * *
    (b) * * *
    (5) * * *
    (vi) Ounces with an appropriate visual unit of measure, as 
described in paragraph (b)(5)(iii) of this section, may be used for 
products that naturally vary in size as provided for in paragraph 
(b)(2)(i)(F) of this section.
* * * * *
    (c) * * *
    (2) * * *
    (i) ``Saturated fat,'' or ``Saturated'': A statement of the number 
of grams of saturated fat in a serving defined as the sum of all fatty 
acids containing no double bonds, except that label declaration of 
saturated fat content information is not required for products that 
contain less than 0.5 gram of total fat in a serving if no claims are 
made about fat, fatty acid, or cholesterol content, and if ``calories 
from saturated fat'' is not declared. Except as provided for in 
paragraph (f) of this section, if a statement of the saturated fat 
content is not required and, as a result, not declared, the statement 
``Not a significant source of saturated fat'' shall be placed at the 
bottom of the table of nutrient values. Saturated fat content shall be 
indented and expressed as grams per serving to the nearest 0.5 gram 
(\1/2\) gram increment below 5 grams and to the nearest gram increment 
above 5 grams. If the serving contains less than 0.5 gram, the content 
shall be expressed as zero.
    (ii) ``Trans fat'' or ``Trans'': A statement of the number of grams 
of trans fat in a serving, defined as the sum of all unsaturated fatty 
acids that contain one or more isolated (i.e., nonconjugated) double 
bonds in a trans configuration, except that label declaration of trans 
fat content information is not required for products that contain less 
than 0.5 gram of total fat in a serving if no claims are made about 
fat, fatty acid or cholesterol content. The word ``trans'' may be 
italicized to indicate its Latin origin. Trans fat content shall be 
indented and expressed as grams per serving to the nearest 0.5 (\1/2\)-
gram increment below 5 grams and to the nearest gram increment above 5 
grams. If the serving contains less than 0.5 gram, the content, when 
declared, shall be expressed as zero. Except as provided for in 
paragraph (f) of this section, if a statement of the trans fat content 
is not required and, as a result, not declared, the statement ``Not a 
significant source of trans fat'' shall be placed at the bottom of the 
table of nutrient values.
    (iii) ``Polyunsaturated fat'' or ``Poly-unsaturated'' (VOLUNTARY): 
A statement of the number of grams of polyunsaturated fat in a serving 
defined as cis,cis-methylene-interrupted

[[Page 65498]]

polyunsaturated fatty acids may be declared voluntarily, except that 
when monounsaturated fat is declared, or when a claim about fatty acids 
or cholesterol is made on the label or in labeling of a food other than 
one that meets the criteria in Sec.  101.62(b)(1) for a claim for ``fat 
free,'' label declaration of polyunsaturated fat is required. 
Polyunsaturated fat content shall be indented and expressed as grams 
per serving to the nearest 0.5 (\1/2\) gram increment below 5 grams and 
to the nearest gram increment above 5 grams. If the serving contains 
less than 0.5 gram, the content shall be expressed as zero.
    (iv) ``Monounsaturated fat'' or ``Monounsaturated'' (VOLUNTARY): A 
statement of the number of grams of monounsaturated fat in a serving 
defined as cis-monounsaturated fatty acids may be declared voluntarily 
except that when polyunsaturated fat is declared, or when a claim about 
fatty acids or cholesterol is made on the label or in labeling of a 
food other than one that meets the criteria in Sec.  101.62(b)(1) for a 
claim for ``fat free,'' label declaration of monounsaturated fat is 
required. Monounsaturated fat content shall be indented and expressed 
as grams per serving to the nearest 0.5 (\1/2\) gram increment below 5 
grams and to the nearest gram increment above 5 grams. If the serving 
contains less than 0.5 gram, the content shall be expressed as zero.
* * * * *
    (6) * * *
    (i) ``Dietary fiber'': A statement of the number of grams of total 
dietary fiber in a serving, indented and expressed to the nearest gram, 
except that if a serving contains less than 1 gram, declaration of 
dietary fiber is not required or, alternatively, the statement 
``Contains less than 1 gram'' or ``less than 1 gram'' may be used, and 
if the serving contains less than 0.5 gram, the content may be 
expressed as zero. Dietary fiber is defined as non-digestible soluble 
and insoluble carbohydrates (with 3 or more monomeric units), and 
lignin that are intrinsic and intact in plants; isolated or synthetic 
non-digestible carbohydrates (with 3 or more monomeric units) 
determined by FDA to have physiological effects that are beneficial to 
human health. Except as provided for in paragraph (f) of this section, 
if dietary fiber content is not required, and as a result not declared, 
the statement ``Not a significant source of dietary fiber'' shall be 
placed at the bottom of the table of nutrient values in the same type 
size. The following isolated or synthetic nondigestible carbohydrate(s) 
have been determined by FDA to have physiological effects that are 
beneficial to human health and, therefore, shall be included in the 
calculation of the amount of dietary fiber: [beta]-glucan soluble fiber 
(as described in Sec.  101.81(c)(2)(ii)(A)), psyllium husk (as 
described in Sec.  101.81(c)(2)(ii)(B)(1)), cellulose, guar gum, 
pectin, locust bean gum, and hydroxypropylmethylcellulose. The 
manufacturer must make and keep records in accordance with paragraphs 
(g)(10) and (11) of this section to verify the declared amount of 
dietary fiber in the label and labeling of food when a mixture of 
dietary fiber, and added nondigestible carbohydrate(s) that does not 
meet the definition of dietary fiber, is present in the food.
* * * * *
    (iii) ``Added Sugars'': A statement of the number of grams of added 
sugars in a serving, except that label declaration of added sugars 
content is not required for products that contain less than 1 gram of 
added sugars in a serving if no claims are made about sweeteners, 
sugars, added sugars, or sugar alcohol content. Except as provided for 
in paragraph (f) of this section, if a statement of the added sugars 
content is not required and, as a result, not declared, the statement 
``Not a significant source of added sugars'' shall be placed at the 
bottom of the table of nutrient values in the same type size. Added 
sugars are either added during the processing of foods, or are packaged 
as such, and include sugars (free, mono and disaccharides), sugars from 
syrups and honey, and sugars from concentrated fruit or vegetable 
juices that are in excess of what would be expected from the same 
volume of 100 percent fruit or vegetable juice of the same type, except 
that fruit or vegetable juice concentrated from 100 percent juices sold 
to consumers, fruit or vegetable juice concentrates used towards the 
total juice percentage label declaration under Sec.  101.30 or for Brix 
standardization under Sec.  102.33(g)(2) of this chapter, fruit juice 
concentrates which are used to formulate the fruit component of 
jellies, jams, or preserves in accordance with the standard of 
identities set forth in Sec. Sec.  150.140 and 150.160 of this chapter, 
or the fruit component of fruit spreads shall not be labeled as added 
sugars. Added sugars content shall be indented under Total Sugars and 
shall be prefaced with the word ``Includes'' followed by the amount (in 
grams) ``Added Sugars'' (``Includes `X' g Added Sugars''). It shall be 
expressed to the nearest gram, except that if a serving contains less 
than 1 gram, the statement ``Contains less than 1 gram'' or ``less than 
1 gram'' may be used as an alternative, and if the serving contains 
less than 0.5 gram, the content may be expressed as zero. When a 
mixture of naturally occurring and added sugars is present in the food, 
and for specific foods containing added sugars, alone or in combination 
with naturally occurring sugars, where the added sugars are subject to 
fermentation and/or non-enzymatic browning, the manufacturer must make 
and keep records in accordance with paragraphs (g)(10) and (11) of this 
section to verify the declared amount of added sugars in the label and 
labeling of food.
* * * * *
    (8) * * *
    (ii) The declaration of vitamins and minerals as a quantitative 
amount by weight and percent of the RDI shall include vitamin D, 
calcium, iron, and potassium in that order, for infants through 12 
months, children 1 through 3 years of age, pregnant women, lactating 
women, and adults and children 4 or more years of age, except 
quantitative weights for these vitamins and minerals are not required 
for labels described in paragraph (j)(13) of this section. The 
declaration of folic acid shall be included as a quantitative amount by 
weight when added as a nutrient supplement or a claim is made about the 
nutrient. The declaration of vitamins and minerals in a food, as a 
quantitative amount by weight and percent of the RDI, may include any 
of the other vitamins and minerals listed in paragraph (c)(8)(iv) of 
this section. The declaration of vitamins and minerals shall include 
any of the other vitamins and minerals listed in paragraph (c)(8)(iv) 
of this section as a statement of the amount per serving of the 
vitamins and minerals as described in this paragraph (c)(8)(ii), 
calculated as a percent of the RDI and expressed as a percent of the 
Daily Value, when they are added as a nutrient supplement, or when a 
claim is made about them, unless otherwise stated as quantitative 
amount by weight and percent of the Daily Value. Other vitamins and 
minerals need not be declared if neither the nutrient nor the component 
is otherwise referred to on the label or the labeling or advertising 
and the vitamins and minerals are:
* * * * *
    (iv) The following RDIs, nomenclature, and units of measure are 
established for the following vitamins and minerals which are essential 
in human nutrition:

[[Page 65499]]



--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                                        RDI
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                            Adults and      Infants \1\     Children 1    Pregnant women
                    Nutrient                                 Unit of measure               children >= 4    through 12       through 3     and lactating
                                                                                               years          months           years           women
--------------------------------------------------------------------------------------------------------------------------------------------------------
Vitamin D......................................  Micrograms (mcg) \2\...................              20              10              15              15
Calcium........................................  Milligrams (mg)........................           1,300             260             700           1,300
Iron...........................................  Milligrams (mg)........................              18              11               7              27
Potassium......................................  Milligrams (mg)........................           4,700             700           3,000           5,100
Vitamin A......................................  Micrograms RAE \3\ (mcg)...............             900             500             300           1,300
Vitamin C......................................  Milligrams (mg)........................              90              50              15             120
Vitamin E......................................  Milligrams (mg) \4\....................              15               5               6              19
Vitamin K......................................  Micrograms (mcg).......................             120             2.5              30              90
Thiamin........................................  Milligrams (mg)........................             1.2             0.3             0.5             1.4
Riboflavin.....................................  Milligrams (mg)........................             1.3             0.4             0.5             1.6
Niacin.........................................  Milligrams NE \5\ (mg).................              16               4               6              18
Vitamin B6.....................................  Milligrams (mg)........................             1.7             0.3             0.5             2.0
Folate \6\.....................................  Micrograms DFE \7\ (mcg)...............             400              80             150             600
Vitamin B12....................................  Micrograms (mcg).......................             2.4             0.5             0.9             2.8
Biotin.........................................  Micrograms (mcg).......................              30               6               8              35
Pantothenic acid...............................  Milligrams (mg)........................               5             1.8               2               7
Phosphorus.....................................  Milligrams (mg)........................           1,250             275             460           1,250
Iodine.........................................  Micrograms (mcg).......................             150             130              90             290
Magnesium......................................  Milligrams (mg)........................             420              75              80             400
Zinc...........................................  Milligrams (mg)........................              11               3               3              13
Selenium.......................................  Micrograms (mcg).......................              55              20              20              70
Copper.........................................  Milligrams (mg)........................             0.9             0.2             0.3             1.3
Manganese......................................  Milligrams (mg)........................             2.3             0.6             1.2             2.6
Chromium.......................................  Micrograms (mcg).......................              35             5.5              11              45
Molybdenum.....................................  Micrograms (mcg).......................              45               3              17              50
Chloride.......................................  Milligrams (mg)........................           2,300             570           1,500           2,300
Choline........................................  Milligrams (mg)........................             550             150             200             550
Protein........................................  Grams (g)..............................             N/A              11             N/A          \8\ 71
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ RDIs are based on dietary reference intake recommendations for infants through 12 months of age.
\2\ The amount of vitamin D may, but is not required to, be expressed in international units (IU), in addition to the mandatory declaration in mcg. Any
  declaration of the amount of vitamin D in IU must appear in parentheses after the declaration of the amount of vitamin D in mcg.
\3\ RAE = Retinol activity equivalents; 1 microgram RAE = 1 microgram retinol, 2 microgram supplemental [beta]-carotene, 12 micrograms dietary [beta]-
  carotene, or 24 micrograms dietary [alpha]-carotene, or dietary 24 micrograms dietary [beta]-cryptoxanthin.
\4\ 1 mg [alpha]-tocopherol (label claim) = 1 mg [alpha]-tocopherol = 1 mg RRR- [alpha]-tocopherol = 2 mg all rac-[alpha]-tocopherol.
\5\ NE = Niacin equivalents, 1 mg NE = 1 mg niacin = 60 milligrams tryptophan.
\6\ ``Folate'' and ``Folic Acid'' must be used for purposes of declaration in the labeling of conventional foods and dietary supplements. The
  declaration for folate must be in mcg DFE (when expressed as a quantitative amount by weight in a conventional food or a dietary supplement), and
  percent DV based on folate in mcg DFE. Folate may be expressed as a percent DV in conventional foods. When folic acid is added or when a claim is made
  about the nutrient, folic acid must be declared in parentheses, as mcg of folic acid.
\7\ DFE = Dietary Folate Equivalents; 1 DFE = 1 mcg naturally occurring folate = 0.6 mcg folic acid.
\8\ Based on the reference caloric intake of 2,000 calories for adults and children aged 4 years and older, and for pregnant women and lactating women.

* * * * *
    (d)(1) * * *
    (iii) Information required in paragraphs (d)(7) and (8) of this 
section shall be in type size no smaller than 8 point. Information 
required in paragraph (d)(5) of this section for the ``Calories'' 
declaration shall be highlighted in bold or extra bold and shall be in 
a type size no smaller than 16 point except the type size for this 
information required in the tabular displays as shown in paragraphs 
(d)(11), (e)(6)(ii), and (j)(13)(ii)(A)(1) of this section and the 
linear display for small packages as shown in paragraph 
(j)(13)(ii)(A)(2) of this section shall be in a type size no smaller 
than 10 point. The numeric amount for the information required in 
paragraph (d)(5) of this section shall also be highlighted in bold or 
extra bold type and shall be in a type size no smaller than 22 point, 
except the type size for this information required for the tabular 
display for small packages as shown in paragraph (j)(13)(ii)(A)(1) of 
this section, and for the linear display for small packages as shown in 
paragraph (j)(13)(ii)(A)(2) of this section no smaller than 14 point. 
The information required in paragraphs (d)(4), (6), and (9) of this 
section shall be in a type size no smaller than 6 point. When provided, 
the information described in paragraph (d)(10) of this section shall be 
in a type size no smaller than 6 point.
* * * * *
    (e) * * *
    (5) The following sample label illustrates the provisions of 
paragraph (e) of this section:

[[Page 65500]]

[GRAPHIC] [TIFF OMITTED] TR21DE18.010

    (6) * * *
    (i) Nutrient information for vitamins and minerals shall be 
separated from information on other nutrients by a bar and shall be 
arrayed vertically in the following order: Vitamin D, calcium, iron, 
and potassium as shown in the following sample labels.

[[Page 65501]]

[GRAPHIC] [TIFF OMITTED] TR21DE18.011


[[Page 65502]]


[GRAPHIC] [TIFF OMITTED] TR21DE18.012

    (ii) The following sample label illustrates the provisions of 
paragraphs (b)(2)(i)(D) and (b)(12)(i) of this section for labels that 
use the tabular display.
[GRAPHIC] [TIFF OMITTED] TR21DE18.013

* * * * *
    (j) * * *
    (13)(i) * * *
    (A) The manufacturer, packer, or distributor shall provide on the 
label of packages that qualify for and use this exemption an address or 
telephone number that a consumer can use to obtain the required 
nutrition information (e.g., ``For nutrition information, call 1-800-
123-4567'').
    (B) When such products bear nutrition labeling, either voluntarily 
or because nutrition claims or other nutrition information is provided, 
all required information shall be in type size no smaller than 6 point 
or all upper-case type of 1-16 inches minimum height, except that 
individual serving-size packages of food served with meals in 
restaurants, institutions, and on board passenger carriers, and not 
intended for sale at retail, may comply with Sec.  101.2(c)(2).
* * * * *

0
3. In Sec.  101.36 revise paragraphs (b)(2)(i)(B) introductory text, 
(b)(2)(ii)(B), (e) introductory text, (e)(11)(ii) and (iv), and (e)(12) 
to read as follows:


Sec.  101.36  Nutrition labeling of dietary supplements.

* * * * *
    (b) * * *
    (2) * * *
    (i) * * *
    (B) The names of dietary ingredients that are declared under 
paragraph (b)(2)(i) of this section shall be presented in a column 
aligned on the

[[Page 65503]]

left side of the nutritional label in the order and manner of 
indentation specified in Sec.  101.9(c), except that calcium and iron 
shall follow choline, and sodium and potassium shall follow chloride. 
This results in the following order for vitamins and minerals: Vitamin 
A, vitamin C, vitamin D, vitamin E, vitamin K, thiamin, riboflavin, 
niacin, vitamin B6, folate and folic acid, vitamin B12, biotin, 
pantothenic acid, choline, calcium, iron, phosphorus, iodine, 
magnesium, zinc, selenium, copper, manganese, chromium, molybdenum, 
chloride, sodium, potassium, and fluoride. The (b)(2)-dietary 
ingredients shall be listed according to the nomenclature specified in 
Sec.  101.9 or in paragraph (b)(2)(i)(B)(2) of this section.
* * * * *
    (ii) * * *
    (B) The amounts of vitamins and minerals, excluding sodium, shall 
be the amount of the vitamin or mineral included in one serving of the 
product, using the units of measurement and the levels of significance 
given in Sec.  101.9(c)(8)(iv), except that zeros following decimal 
points may be dropped, and additional levels of significance may be 
used when the number of decimal places indicated is not sufficient to 
express lower amounts (e.g., the RDI for zinc is given in whole 
milligrams (mg), but the quantitative amount may be declared in tenths 
of a mg). The amount of vitamin D may, but is not required to, be 
expressed in IUs, in addition to the mandatory declaration in mcg. Any 
declaration of the amount of vitamin D in IUs must appear in 
parentheses after the declaration of the amount of vitamin D in mcg.
* * * * *
    (e) Except as provided for small and intermediate sized packages 
under paragraph (h)(3)(i)(2) of this section, information other than 
the title, headings, and footnotes shall be in uniform type size no 
smaller than 8 point. Type size no smaller than 6 point may be used for 
column headings (e.g., ``Amount Per Serving'' and ``% Daily Value'') 
and for footnotes (e.g., ``Percent Daily Values are based on a 2,000 
calorie diet'').
* * * * *
    (11) * * *
    (ii) Multiple vitamins for children and adults (excludes Servings 
Per Container which is stated in the net quantity of contents 
declaration):
[GRAPHIC] [TIFF OMITTED] TR21DE18.014

* * * * *
    (iv) Dietary supplement containing dietary ingredients with and 
without RDIs and DRVs:

[[Page 65504]]

[GRAPHIC] [TIFF OMITTED] TR21DE18.015

* * * * *
    (12) If space is not adequate to list the required information as 
shown in the sample labels in paragraph (e)(11) of this section, the 
list may be split and continued to the right as long as the headings 
are repeated. The list to the right must be set off by a line that 
distinguishes it and sets it apart from the dietary ingredients and 
percent of Daily Value information given to the left. The following 
sample label illustrates this display:
[GRAPHIC] [TIFF OMITTED] TR21DE18.016

* * * * *

0
4. Revise appendix B to part 101 to read as follows:

Appendix B to Part 101--Graphic Enhancements Used by the FDA

[[Page 65505]]

[GRAPHIC] [TIFF OMITTED] TR21DE18.017


[[Page 65506]]


[GRAPHIC] [TIFF OMITTED] TR21DE18.018


    Dated: December 13, 2018.
Scott Gottlieb,
Commissioner of Food and Drugs.
[FR Doc. 2018-27431 Filed 12-19-18; 8:45 am]
 BILLING CODE 4164-01-P
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