Food Labeling: Notification Procedures for Statements on Dietary Supplements

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form FDA 3955 Notification Procedures for Statements on Dietary Supplements	Form	Unchanged	Repair queued
Form FDA 3955 Certain Types of Statements for Dietary Supplements	Form	Unchanged	Repair queued
0331 Dietary Supp Labeling SSA 2025 EXT.docx	Supporting Statement A	Uploaded 2025-07-30	Repair queued
0331 Dietary Supp Labeling SSA 2025 EXT.docx	Supporting Statement A	Uploaded 2025-07-30	Repair queued
0910-0331 response to comment.docx	Supplementary Document	Uploaded 2022-07-14	Repair queued
0910-0331 response to comment.docx	Supplementary Document	Uploaded 2022-07-14	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
5918	Certain Types of Statements for Dietary Supplements	Form	Unchanged	Notification Procedures for Statements on Dietary Supplements
5918	Certain Types of Statements for Dietary Supplements	Form	Unchanged

ICR Details

OMB Control No: 0910-0331	ICR Reference No: 202411-0910-001
Status: Active	Previous ICR Reference No: 202111-0910-005
Agency/Subagency: HHS/FDA	Agency Tracking No: HFP
Title: Food Labeling: Notification Procedures for Statements on Dietary Supplements
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 09/02/2025
Retrieve Notice of Action (NOA)	Date Received in OIRA: 07/30/2025
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2028	36 Months From Approved	08/31/2025
Responses	3,690	0	3,690
Time Burden (Hours)	2,768	0	2,768
Cost Burden (Dollars)	0	0	0

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Abstract: The reporting requirements of this regulation implement the Dietary Supplement Health and Education Act. The subject regulation establishes reporting procedures necessary to inform FDA when dietary supplement manufacturers are making statements of nutritional support on their labels or in their labeling. FDA is seeking OMB approval of an electronic submission method for this collection.

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Authorizing Statute(s): US Code: 21 USC 343(r)(6) Name of Law: Federal Food, Drug, and Cosmetic Act; Misbranding
  

Citations for New Statutory Requirements: None

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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:
	90 FR 18665	05/01/2025
30-day Notice:	Federal Register Citation:	Citation Date:
	90 FR 35694	07/29/2025
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

table that charts list of burden

IC Title	Form No.	Form Name
Certain Types of Statements for Dietary Supplements	FDA 3955	Notification Procedures for Statements on Dietary Supplements

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ICR Summary of Burden

table that charts list of burden

	Total Approved	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	3,690	3,690	0	0	0	0
Annual Time Burden (Hours)	2,768	2,768	0	0	0	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:

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Annual Cost to Federal Government: $159,300

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.     No

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: 07/30/2025

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