Safety Standard for Infant Sleep Products

Forms and Documents

Document Name	Status
PRA Supporting statement for Infant Sleep Products-Final Rule.pdf Supporting Statement A	2021-06-23

IC Document Collections

IC ID	Document Title	Status
226614	Third-Party Disclosure Requirements for Instructional Literature in the Safety Standard for Infant Sleep Products	Modified
226613	Third-Party Disclosure Requirements for Labeling and Marking in the Safety Standard for Infant Sleep Products	Modified

ICR Details

OMB Control No: 3041-0177	ICR Reference No: 202105-3041-002
Status: Received in OIRA	Previous ICR Reference No: 201704-3041-007
Agency/Subagency: CPSC	Agency Tracking No:
Title: Safety Standard for Infant Sleep Products
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 06/23/2021

	Requested	Previously Approved
Expiration Date	36 Months From Approved
Responses	3,850	0
Time Burden (Hours)	68,650	0
Cost Burden (Dollars)	0	0

---

Abstract: As directed by statutory requirement, the Commission is promulgating a safety standard for infant sleep products. The final rule defines an “infant sleep product” as a product marketed or intended to provide a sleeping accommodation for an infant up to 5 months of age, and that is not already subject to one of the mandatory CPSC sleep standards. The infant sleep products covered by this rule include inclined and flat sleep products, such as inclined sleepers, play yard infant sleep accessories, baby nests and pods, in-bed sleepers, baby hammocks, compact or travel bassinets without a stand or legs, and baby tents. This final rule for infant sleep products incorporates by reference the voluntary standard for infant inclined sleep products issued by ASTM International, with modifications to further reduce the risk of injury associated with infant sleep products. The Safety Standard for Infant Sleep Products includes performance and labeling requirements for marking, labeling, and instructional literature. These requirements fall within the definition of “collection of information,” as defined in 44 U.S.C. 3502(3).

---

Authorizing Statute(s): PL: Pub.L. 110 - 314 104(b) Name of Law: Consumer Product Safety Improvement Act of 2008 (CPSIA)
  

Citations for New Statutory Requirements: PL: Pub.L. 110 - 314 104(b) Name of Law: CPSIA

---

Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
3041-AD45	Final or interim final rulemaking	86 FR 33022	06/23/2021

---

Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

---

Number of Information Collection (IC) in this ICR: 2

IC Title	Form No.	Form Name
Third-Party Disclosure Requirements for Instructional Literature in the Safety Standard for Infant Sleep Products
Third-Party Disclosure Requirements for Labeling and Marking in the Safety Standard for Infant Sleep Products

---

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	3,850	0	3,850	0	0	0
Annual Time Burden (Hours)	68,650	0	68,650	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: New Rule under the 2008 CPSIA.

---

Annual Cost to Federal Government: $4,166

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

---

Common Form ICR:  No

---

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: 06/23/2021

---