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Night Time Cold and Flu Relief

NDC 69842-899 · CVS Pharmacy

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

69842-899-16 — 16 BLISTER PACK in 1 CARTON (69842-899-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

69842-899-24 — 24 BLISTER PACK in 1 CARTON (69842-899-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

69842-899-48 — 48 BLISTER PACK in 1 CARTON (69842-899-48) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-800 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 69842-812 — guaifenesin, dextromethorphan HBr, 69842-819 — Dextromethorphan HBr, Guaifenesin, 69842-847 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 69842-848 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 69842-864 — Acetaminophen, 69842-876 — Acetaminophen, 69842-878 — Acetaminophen, 69842-886 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 69842-897 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL, 69842-903 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-904 — Dextromethorphan Hydrobromide Guaifenesin, 69842-915 — Acetaminophen, 69842-926 — Dextromethorphan HBr, Guaifenesin, 69842-930 — Acetaminophen, 69842-931 — Acetaminophen, 69842-933 — Guaifenesin, Dextromethorphan HBr, 69842-937 — Dextromethorphan HBr and Guaifenesin, 69842-942 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-947 — Acetaminophen, Dextromethorphan HBr, +4482 more

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