Skip to main content

Walgreens Childrens

NDC 0363-7560 · WALGREENS CO.

Generic nameNighttime Cough
Dosage formLIQUID
RouteORAL
Active ingredient(s)CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE
Strength2; 15 mg/10mL; mg/10mL
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], 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

0363-7560-04 — 118 mL in 1 BOTTLE (0363-7560-04)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-6812 — dextromethorphan hydrobromide, guaifenesin, 0363-6980 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 0363-7270 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL, 0363-7296 — Dextromethorphan Hydrobromide and Guaifenesin, 0363-7380 — Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, 0363-7389 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-7390 — Dextromethorphan HBr and Guaifenesin, 0363-7440 — dextromethorphan hydrobromide and guaifenesin, 0363-7470 — Children Cough and Chest Congestion, 0363-7550 — Cough and Chest Congestion, 0363-7754 — Dextromethorphan HBr, Guaifenesin, 0363-7760 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0363-7920 — Acetaminophen, Chlorpheniramine Maleate, and Dextromethorphan Hydrobromide, 0363-8004 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-8005 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-8031 — Dextromethorphan HBr, Guaifenesin, 0363-8063 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 0363-8078 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Triprolidine HCl, 0363-8100 — acetaminophen, dextromethorphan hydrobromide, 0363-8990 — DEXTROMETHORPHAN HBr, +2124 more

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