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Daytime Severe Cold and Cough

NDC 37808-718 · H E B

Generic nameAcetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength650; 20; 10 mg/30mL; mg/30mL; mg/30mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

37808-718-83 — 245 mL in 1 BOTTLE, PLASTIC (37808-718-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-574 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-586 — Acetaminophen, Aspirin, Caffeine, 37808-594 — Dextromethorphan HBr, Guaifensin, 37808-598 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 37808-628 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 37808-639 — Dextromethorphan HBr, Guaifenesin, 37808-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 37808-663 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-704 — Acetaminophen, 37808-728 — Phenylephrine hydrochloride, 37808-730 — Guaifenesin, Dextromethorphan HBr, 37808-733 — Guaifenesin, Dextromethorphan HBr, 37808-747 — Acetaminophen, 37808-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 37808-775 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-792 — Acetaminophen, 37808-795 — Acetaminophen and Diphenhydramine Hydrochloride, 37808-811 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 37808-834 — Guaifenesin, Dextromethorphan HBr, +4867 more

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