[NCCDPHP] List of Ingredients Added to Tobacco in the Manufacture of Cigarette Products

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Recommended Cigarette Ingredient Reporting Format - FCLAA	Form and Instruction	Modified	Available
0210 PN.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 7 Human Subjects Non-research Determ.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 6b Civil Penalties for Disclosure of Confidential Info (18 U.S.C. 1905).pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 6a Privileged Information Guidelines.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 5 Initial FRN (1985).pdf	Supplementary Document	Uploaded 2026-05-05	Available
Att 4 60 Day FRN.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 3b Recommencement of Reporting Require.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 Att 3a Change in Reporting Require.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0210 Att 2 Compliance Cert Manufacs Pkgers & Importers of Tobacco Products.pdf	Supplementary Document	Uploaded 2026-05-05	Available
0210 Att 1b Fed Cig Labeling and Ad Act (15 U.S.C. 1331-1341).pdf	Supplementary Document	Uploaded 2026-05-05	Available
0210 Att 1a Comp Smoking Education Act of 1984 (15 U.S.C. 1335a).pdf	Supplementary Document	Uploaded 2026-05-05	Available
0920 0210 SSA_final.docx	Supporting Statement A	Uploaded 2026-05-05	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
183310	Ingredient Report	Form and Instruction	Modified	Recommended Cigarette Ingredient Reporting Format - FCLAA

ICR Details

OMB Control No: 0920-0210	ICR Reference No: 202604-0920-005
Status: Received in OIRA	Previous ICR Reference No: 202203-0920-015
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-26-0188
Title: [NCCDPHP] List of Ingredients Added to Tobacco in the Manufacture of Cigarette Products
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 05/07/2026

table that charts list comparision

	Requested	Previously Approved
Expiration Date	36 Months From Approved
Responses	55	0
Time Burden (Hours)	358	0
Cost Burden (Dollars)	0	0

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Abstract: This is a legislatively mandated information collection. As required by the Federal Cigarette Labeling and Advertising Act (15 U.S.C. 1335a(a), or P.L .89-92), CDC's Office on Smoking and Health collects information from cigarette manufacturers, packagers and importers about the ingredients used in cigarette products. This collection is commonly known as the Ingredient Report. This is a reinstatement with very minor changes.

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Authorizing Statute(s): PL: Pub.L. 98 - 474 1341 Name of Law: Comprehensive Smoking Education Act
   US Code: 15 USC 1331 Name of Law: Federal Cigarette Labeling and Advertising Act
  

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 43448	09/09/2025
30-day Notice:	Federal Register Citation:	Citation Date:
	91 FR 24241	05/05/2026
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
Ingredient Report	n/a	Recommended Cigarette Ingredient Reporting Format - FCLAA

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ICR Summary of Burden

table that charts list 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	55	0	0	55	0	0
Annual Time Burden (Hours)	358	0	0	358	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

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

Burden Reduction Due to:

Short Statement: This is a Reinstatement.

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Annual Cost to Federal Government: $12,490

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: 05/07/2026

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