United States · FDA National Drug Code directory
Zyrtec Allergy
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50580-754_3a6e2ec1-eab8-beec-e063-6394a90aa39c
- Product NDC
- 50580-754
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Kenvue Brands LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20250215
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 POUCH in 1 CARTON (50580-754-15) / 1 TABLET, FILM COATED in 1 POUCH · 50580-754-15
- 1 BOTTLE in 1 CARTON (50580-754-35) / 35 TABLET, FILM COATED in 1 BOTTLE · 50580-754-35
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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