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Night Time Cold and Flu Relief

NDC 11822-3335 · Rite Aid Corporation

Generic nameAcetaminophen, Dextromethorphan HBr, 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

11822-3335-5 — 24 BLISTER PACK in 1 CARTON (11822-3335-5) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-1590 — Acetaminophen, Aspirin and caffeine, 11822-1630 — dextromethorphan hydrobromide, guaifenesin, 11822-1812 — dextromethorphan HBr, guaifenesin, 11822-1987 — ACETAMINOPHEN 325 mg DEXTROMETHORPHAN HBr 15 mg DOXYLAMINE SUCCINATE 6.25 mg, 11822-1989 — ACETAMINOPHEN 325 mg DEXTROMETHORPHAN HBr 10 mg PHENYLEPHRINE HCI 5 mg, 11822-2219 — dextromethorphan hydrobromide, guaifenesin, 11822-2350 — Acetaminophen and Diphenhydramine HCl, 11822-3000 — Doxylamine Succinate, 11822-3120 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 11822-3318 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-3343 — Aspirin, Acetaminophen, Caffeine, 11822-3391 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 11822-3392 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 11822-3900 — Acetaminophen, Caffeine, Pyrilamine maleate, 11822-4099 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 11822-4450 — acetaminophen, 11822-4484 — Acetaminophen, 11822-4669 — Acetaminophen, Phenylephrine HCl, 11822-5019 — Acetaminophen, 11822-5022 — Acetaminophen and Phenylephrine HCl, +4482 more

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