United States · FDA National Drug Code directory
all day 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
- 11822-1002_203e5940-cdf3-4191-83ab-af83d393e82f
- Product NDC
- 11822-1002
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Rite Aid Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210914 / 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 BLISTER PACK in 1 CARTON (11822-1002-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 11822-1002-1
- 1 BOTTLE in 1 CARTON (11822-1002-2) / 30 TABLET, FILM COATED in 1 BOTTLE · 11822-1002-2
- 1 BOTTLE in 1 CARTON (11822-1002-3) / 60 TABLET, FILM COATED in 1 BOTTLE · 11822-1002-3
- 1 BOTTLE in 1 CARTON (11822-1002-4) / 120 TABLET, FILM COATED in 1 BOTTLE · 11822-1002-4
- 1 BOTTLE in 1 CARTON (11822-1002-7) / 300 TABLET, FILM COATED in 1 BOTTLE · 11822-1002-7
- 1 BOTTLE in 1 CARTON (11822-1002-8) / 90 TABLET, FILM COATED in 1 BOTTLE · 11822-1002-8
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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