Skip to main content

Mucus Congestion and Cough Relief

NDC 0363-0512 · Walgreens

Generic nameDextromethorphan HBr, Guaifensin, Phenylephrine HCI
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength5; 100; 2.5 mg/5mL; mg/5mL; mg/5mL
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

0363-0512-06 — 1 BOTTLE, PLASTIC in 1 BOX (0363-0512-06) / 201 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-0384 — dextromethorphan polistirex, 0363-0401 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0363-0437 — Guaifenesin, Dextromethorphan HBr, 0363-0460 — Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI, 0363-0474 — Guaifenesin and Dextromethorphan HBr, 0363-0476 — Hemorrhoidal Rectal Suppositories, 0363-0479 — Hemorrhoidal Rectal Suppositories, 0363-0494 — dextromethorphan polistirex, 0363-0506 — Dextromethorphan HBr, Guaifenesin, 0363-0510 — Guaifenesin and Dextromethorphan HBr, 0363-0532 — Guaifenesin, 0363-0533 — Dextromethorphan HBr, Guaifenesin, 0363-0542 — Guaifenesin, Phenylephrine HCl, 0363-0559 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl, 0363-0566 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0363-0570 — Guaifenesin, 0363-0603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 0363-0623 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 0363-0640 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-0641 — Hemorrhoidal Cream, +3082 more

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