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Federal regulations · Through 2026-08-25 · Newer source version available

10 CFR 35.69: Labeling of vials and syringes.

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Where this section sits in the code
  1. Title 10—Energy
  2. CHAPTER I—NUCLEAR REGULATORY COMMISSION
  3. PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
  4. Subpart C—General Technical Requirements

Each syringe and vial that contains unsealed byproduct material must be labeled to identify the radioactive drug. Each syringe shield and vial shield must also be labeled unless the label on the syringe or vial is visible when shielded.

Collected 2026-08-27T02:24:09Z. Source file · JSON

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