Lead in General Industry Standard (29 CFR 1910.1025)

Forms and Documents

Document Name	Status
SS_1218-0092_Lead in General industry _2025_ROCIS.docx Supporting Statement A	2025-12-03
60_Day_FRN_OSHA-2012-0013-0013_4-14-2025.pdf Supplementary Document	2025-06-06
29 CFR 1910.1025_4-25-2025.docx Supplementary Document	2025-06-06
OSH Act Section 8 USC 657.pdf Supplementary Document	2025-06-06
OSH Act Section 6 USC 655 (2).pdf Supplementary Document	2025-06-06
OSH Act Section 2 USC 651 (2).pdf Supplementary Document	2025-06-06

IC Document Collections

IC ID	Document Title	Status
14001	Lead in General Industry Standard (29 CFR 1910.1025)	Modified

ICR Details

OMB Control No: 1218-0092	ICR Reference No: 202506-1218-001
Status: Received in OIRA	Previous ICR Reference No: 202302-1218-002
Agency/Subagency: DOL/OSHA	Agency Tracking No: 1218-0092 (2025)
Title: Lead in General Industry Standard (29 CFR 1910.1025)
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 12/08/2025

	Requested	Previously Approved
Expiration Date	36 Months From Approved	04/30/2026
Responses	4,042,988	3,886,840
Time Burden (Hours)	1,250,537	1,134,438
Cost Burden (Dollars)	210,232,946	145,080,120

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Abstract: The purpose of this standard and its information collection requirements is to provide protection for workers from the adverse effects associated with occupational exposure to the carcinogen lead. Employers must monitor exposure to lead, provide medical surveillance, train employees about the hazards of lead, and establish and maintain accurate records of worker exposure to lead. These records are used by employers, workers, physicians, and the Government to ensure that workers are not being harmed by exposure to lead.

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Authorizing Statute(s): US Code: 29 USC 651 Name of Law: Occupational Safety and Health Act
   US Code: 29 USC 655 Name of Law: Occupational Safety and Health Act
   US Code: 29 USC 657 Name of Law: Occupational Safety and Health 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 15591	04/14/2025
30-day Notice:	Federal Register Citation:	Citation Date:
	90 FR 56801	12/08/2025
Did the Agency receive public comments on this ICR? Yes

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

IC Title	Form No.	Form Name
Lead in General Industry Standard (29 CFR 1910.1025)

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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	4,042,988	3,886,840	0	0	156,148	0
Annual Time Burden (Hours)	1,250,537	1,134,438	0	0	116,099	0
Annual Cost Burden (Dollars)	210,232,946	145,080,120	0	0	65,152,826	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: The agency is requesting a burden hour adjustment increase of 116,099 hours (from 1,134,438 hours to 1,250,537 hours). The adjustment increase is due to an overall increase in the number of employers (56,906 to 60,569 employers) and an increase in the number of exposed workers (346,894 to 366,629 exposed workers), based on updated data. Also, the agency is requesting an adjustment cost increase of $65,152,826 (from $145,080,120 to $210,232,946). The increase is mainly due to two factors: first, an increase in the number of employees receiving exposure monitoring, biological monitoring, and medical examinations; and second, an increase in costs to perform these exposure, biological, monitoring’s and medical examinations as required by the standard.

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Annual Cost to Federal Government: $0

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: 12/08/2025

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