United States · FDA National Drug Code directory
Up and Up Allergy Relief
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
- 11673-502_8f32f92c-9043-439d-a318-8f4ae6b1ad39
- Product NDC
- 11673-502
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Target Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141217
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (11673-502-00) / 90 TABLET, FILM COATED in 1 BOTTLE · 11673-502-00
- 1 BOTTLE in 1 CARTON (11673-502-39) / 30 TABLET, FILM COATED in 1 BOTTLE · 11673-502-39
- 2 BOTTLE in 1 CARTON (11673-502-48) / 90 TABLET, FILM COATED in 1 BOTTLE (11673-502-75) · 11673-502-48
- 1 BOTTLE in 1 CARTON (11673-502-72) / 60 TABLET, FILM COATED in 1 BOTTLE · 11673-502-72
- 1 BOTTLE in 1 CARTON (11673-502-76) / 120 TABLET, FILM COATED in 1 BOTTLE · 11673-502-76
- 1 BOTTLE in 1 CARTON (11673-502-87) / 300 TABLET, FILM COATED in 1 BOTTLE · 11673-502-87
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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