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Tussin

NDC 70000-0133 · Cardinal Health (Leader) 70000

Generic nameDextromethorphan HBr, Guaifenesin, Phenylephrine HCI
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength20; 200; 10 mg/10mL; mg/10mL; mg/10mL
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

70000-0133-1 — 1 BOTTLE, PLASTIC in 1 BOX (70000-0133-1) / 118 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69848-017 — Guaifenesin, 69848-018 — Guaifenesin, 70000-0046 — Mineral Oil, Petrolatum, Phenylephrine HCI, 70000-0050 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 70000-0055 — Guaifenesin, 70000-0056 — Dextromethorphan Hydrobromide / Guaifenesin, 70000-0057 — Brompheniramine maleate, Phenylephrine HCl, 70000-0080 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70000-0083 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 70000-0132 — Phenylephrine Hydrochloride, 70000-0141 — Guaifenesin, Phenylephrine HCl, 70000-0161 — Acetaminophen, Phenylephrine HCl, 70000-0183 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70000-0184 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70000-0187 — dextromethorphan polistirex, 70000-0191 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 70000-0192 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 70000-0195 — dextromethorphan polistirex, 70000-0211 — Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl, 70000-0223 — cocoa butter, phenylephrine HCl, +3082 more

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