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Hazard communication duties for veterinary drugs

Summary A veterinary laboratory asked how OSHA's hazard communication rule applied to drugs. OSHA said hazardous drugs generally needed material safety data sheets, even where FDA labeling displaced OSHA's label rule, but solid final-form drugs ready for direct administration could be exempt. The source page notes a 2024 correction.
Document
Federal opinion letter
Agency
Occupational Safety and Health Administration (OSHA)
Document number
1993-12-22
Date issued
December 22, 1993
Status
Active
Status last verified October 9, 2026

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About this page: The full text below is the official document from Occupational Safety and Health Administration (OSHA). Ezel adds the plain-English summary and tracks the document's status. The official source linked on this page is authoritative for any reliance.

December 22, 1993

C.M. Stowe, VMD, PhD.
Wendt Professional Laboratories
[Recipient address omitted]
Dear Dr. Stowe:

Thank you for your letter of December 10 concerning the requirements under the Occupational Safety and Health Administration's (OSHA) Hazardous Communication Standard (HCS), 29 CFR 1910.1200 as they apply to veterinary drugs.

The standard does not apply to nonhazardous drugs, but any drug that meets the criteria of a hazardous chemical in the HCS generally would be covered. The HCS contains some exemptions that would apply to some drug and veterinary products. Section (b)(5)(ii) of the HCS states that drugs that are subject to labeling requirements by the Food and Drug Administration (FDA) under the Federal Food, Drug and Cosmetic Act are exempt from the labeling provisions of OSHA's Hazard Communication Standard. Please note that this section of the HCS exempts only labeling requirements and does not exempt the other requirements of the standard such as providing Material Safety Data Sheets (MSDS).

Another section of the standard that is relevant to your situation is 1910.1200(b)(6)(viii) which exempts from coverage under the standard drugs as defined by the Federal Food, Drug and Cosmetic Act that are in solid final form, ready for direct administration to the patient such as tablets, capsules or pills. If these drugs are not in final form in that they are designed to be dissolved or crushed by employees prior to administration, then they are covered by the HCS. (There may be situations where a tablet, capsule or pill is dissolved or crushed for purposes of administration when that is not generally the way it is dispensed. The final form exemption would apply in this situation.) Consequently, MSDS are required to be prepared and transmitted with the initial shipment of all hazardous chemicals including drug and veterinary products, except for products which are in solid final form for direct administration to patient.

As you may be aware, the Occupational Safety and Health Act of 1970 allows states to assume responsibility for their own occupational safety and health plans, which are approved and monitored by Federal OSHA. The Minnesota Department of Industry and Labor operates such a plan. As a condition of plan approval, States are required to adopt and enforce standards that are either identical to, or at least as effective as, the Federal standards. Therefore, this response may differ from that which would be given by the State of Minnesota. For information regarding the requirements of Minnesota standards, you may want to contact:

Minnesota Department of Labor and Industry
443 Lafayette Road
St. Paul, Minnesota 55155
Telephone: (612) 296-2342

We hope this information is helpful. If you have any further questions please contact [the Office of Health Enforcement at (202) 693-2190].

Sincerely,
Roger A. Clark, Director
Directorate of Compliance Programs

------------------------------------------------------------------------

[Corrected 12/6/2024]

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