United States · FDA National Drug Code directory

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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
82501-0422_5d8e3ec6-14de-463d-bea1-d40f50266304
Product NDC
82501-0422
Form
TABLET, FILM COATED
Composition / generic term
Cetirizine Hydrochloride
Labeler
Gobrands, Inc
Marketing category
ANDA
Marketing start / end (source format)
20251027
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 (82501-0422-1) / 30 TABLET, FILM COATED in 1 BOTTLE (82501-0422-0) · 82501-0422-1

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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