Cosmetic Labeling and Voluntary Cosmetic Registration

Forms and Documents

Document Name	Status
0599 Cosmetics SSA 2023 REV for MoCRA.docx Supporting Statement A	2023-09-20

IC Document Collections

IC ID	Document Title	Status
262241	Cosmetic recordkeeping requirements, including Adverse Event records	New
243117	Cosmetic registration and listing Other-Statutory Authority	Modified
178493	Cosmetic disclosure requirements	Modified

ICR Details

OMB Control No: 0910-0599	ICR Reference No: 202309-0910-009
Status: Received in OIRA	Previous ICR Reference No: 202008-0910-008
Agency/Subagency: HHS/FDA	Agency Tracking No: CFSAN
Title: Cosmetic Labeling and Voluntary Cosmetic Registration
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 09/20/2023

	Requested	Previously Approved
Expiration Date	36 Months From Approved	09/30/2023
Responses	253,211	152,429
Time Burden (Hours)	224,056	144,218
Cost Burden (Dollars)	0	0

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Abstract: This information collection supports implementation of statutory and regulatory provisions that govern cosmetics. Respondents to the collections of information include cosmetic manufacturers and processors.

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Authorizing Statute(s): US Code: 21 USC 301 et seq. Name of Law: FFDCA
  

Citations for New Statutory Requirements: PL: Pub.L. 117 - 328 3501 Name of Law: Modernization of Cosmetics Regulation Act of 2022

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	88 FR 26564	05/01/2023
30-day Notice:	Federal Register Citation:	Citation Date:
	88 FR 63960	09/18/2023
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 3

IC Title	Form No.	Form Name
Cosmetic disclosure requirements
Cosmetic recordkeeping requirements, including Adverse Event records
Cosmetic registration and listing	FDA 5066, FDA 5067	Registration of Cosmetic Product Facility ,   Cosmetic Product Listing

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ICR Summary of Burden

	Total Request	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	253,211	152,429	0	0	100,782	0
Annual Time Burden (Hours)	224,056	144,218	0	0	79,838	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: This information collection reflects program changes introduced by new legislation. The burden for this information collection reflects an overall increase of 79,838 burden hours and an increase of 100,782 responses annually.

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Annual Cost to Federal Government: $2,720,010

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     Yes

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? No

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 09/20/2023

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