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Leader Daytime Severe Cold and Flu Relief

NDC 70000-0636 · Cardinal Health 110, LLC. dba Leader

Generic nameacetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Dosage formTABLET, FILM 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

70000-0636-1 — 12 BLISTER PACK in 1 CARTON (70000-0636-1) / 2 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0568 — Acetaminophen and Phenylephrine HCl, 70000-0596 — dextromethorphan hydrobromide, guaifenesin, 70000-0611 — acetaminophen, aspirin, caffeine, 70000-0622 — Acetaminophen and Ibuprofen, 70000-0623 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 70000-0626 — Acetaminophen, 70000-0627 — Acetaminophen, 70000-0628 — Dextromethorphan HBr, Guaifenesin, 70000-0629 — Dextromethorphan HBr, guaifenesin, Phenylephrine HCl, 70000-0630 — Dextromethorphan HBr, Guaifenesin, 70000-0652 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 70000-0670 — Dextromethorphan HBr, Guaifenesin, 70000-0673 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70000-0674 — Acetaminophen, 70000-0696 — Guaifenesin, 70000-0707 — Dextromethorphan HBr, Guaifenesin, 70000-0709 — Acetaminophen, 70000-0713 — dextromethorphan hydrobromide and guaifenesin, 70000-0715 — brompheniramine maleate, dextromethorphan hydrobromide, 70000-0719 — guaifenesin, pseudoephedrine hydrochloride, +5267 more

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