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DAYTIME SEVERE COLD AND FLU

NDC 37808-178 · HEB

Generic nameACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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

37808-178-03 — 2 BLISTER PACK in 1 CARTON (37808-178-03) / 12 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 37808-093 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 37808-095 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 37808-120 — Acetaminophen, 37808-130 — Acetaminophen, 37808-161 — Acetaminophen, 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, 37808-317 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 37808-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 37808-367 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-374 — Acetaminophen, Aspirin, Caffeine, 37808-384 — dextromethorphan polistirex, +5267 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels