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Triacting Daytime Cold Cough

NDC 21130-378 · Safeway, Inc.

Generic nameDextromethorphan HBr, Phenylephrine HCl
Dosage formSYRUP
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength5; 2.5 mg/5mL; mg/5mL
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

21130-378-04 — 1 BOTTLE, PLASTIC in 1 BOX (21130-378-04) / 118 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

17856-1162 — Guaifenesin, Dextromethorphan HBr, 17856-4024 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 17856-6312 — dextromethorphan polistirex, 21130-012 — dextromethorphan polistirex, 21130-036 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 21130-044 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 21130-091 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 21130-129 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 21130-162 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 21130-343 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 21130-379 — Diphenhydramine HCl, Phenylephrine HCl, 21130-385 — Dextromethorphan HBr, Guaifenesin, 21130-436 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 21130-453 — Phenylephrine HCl, 21130-454 — dextromethorphan hydrobromide, guaifenesin, 21130-474 — Acetaminophen, Phenylephrine HCl, 21130-499 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 21130-502 — Acetaminophen, Phenylephrine HCl, 21130-505 — Dextromethorphan HBr, Guaifenesin, 21130-520 — dextromethorphan polistirex, +2670 more

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