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Tampax Pearl

by Procter & Gamble Manufacturing Company, the GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00073010632752 UDI-DIDate12 Aug 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Tampax
Generic Name
Menstrual tampon, unscented
Model / Reference
Tampax Pearl
Primary DI / UDI-DI
00073010632752
FDA Product Code
HEB
GMDN Term
Menstrual tampon, unscented
Device Class
Class II
Regulation Number
884.5470
GUDID distribution status
In Commercial Distribution

Related devices

Category: Menstrual tampon, unscented

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Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No