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Cold and Flu Relief

NDC 21130-849 · Safeway, Inc.

Generic nameACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength325; 15; 6.25 mg/1; mg/1; mg/1
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

21130-849-24 — 24 BLISTER PACK in 1 CARTON (21130-849-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-627 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 21130-650 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 21130-661 — Acetaminophen and Diphenhydramine HCL, 21130-681 — Acetaminophen, Aspirin and Caffeine, 21130-689 — chlorpheniramine maleate, dextromethorphan HBr, 21130-707 — Dextromethorphan HBr, Guaifenesin, 21130-716 — Acetaminophen, Ibuprofen, 21130-719 — Acetaminophen, 21130-738 — Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl, 21130-746 — Acetaminophen, 21130-866 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 21130-890 — Dextromethorphan polistirex, 21130-899 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 21130-900 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 21130-907 — acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate, 21130-909 — Acetaminophen 650 mg, Dextromethorphan HBr 20 mg, Guaifenesin 400 mg, Phenylephrine HCl 10 mg, 21130-910 — Acteminophen, 21130-930 — Acetaminophen, Caffeine, Pyrilamine maleate, 21130-940 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 21130-945 — Acetaminophen, +4482 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.