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NDC 37808-093 · H-E-B

Generic nameAcetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE
Strength325; 10; 5 mg/1; mg/1; mg/1
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

37808-093-16 — 2 BLISTER PACK in 1 CARTON (37808-093-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37000-712 — Phenylephrine Hydrochloride and Diphenhydramine Hydrochloride, 37000-810 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 37000-812 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, and Phenylephrine Hydrochloride, 37000-815 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and phenylephrine hydrochloride, 37000-950 — Acetaminophen, Phenylephrine HCl, 37000-951 — Acetaminophen, Phenylephrine HCl, Guaifenesin, 37000-959 — Dextromethorphan HBr and Guaifenesin, 37000-974 — Diphenhydramine Hydrochloride and Acetaminophen, 37808-056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 37808-062 — Benzocaine, 37808-095 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 37808-120 — Acetaminophen, 37808-130 — Acetaminophen, 37808-161 — Acetaminophen, 37808-178 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-195 — Acetaminophen, 37808-273 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-279 — cocoa butter, phenylephrine HCl, 37808-285 — Acetaminophen, 37808-316 — ACETAMINOPHEN,DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN , PHENYLEPHRINE HCL, +4867 more

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