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Childrens Dibromm Cold and Allergy

NDC 70000-0057 · Cardinal Health (Leader) 70000

Generic nameBrompheniramine maleate, Phenylephrine HCl
Dosage formLIQUID
RouteORAL
Active ingredient(s)BROMPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE
Strength2; 5 mg/10mL; mg/10mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

70000-0057-1 — 1 BOTTLE, PLASTIC in 1 BOX (70000-0057-1) / 118 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-796 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 69842-800 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 69842-848 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 69842-897 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL, 69842-903 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-942 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-966 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDE, 69842-969 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL, 69842-997 — Guaifenesin/phenylephrine, 70000-0046 — Mineral Oil, Petrolatum, Phenylephrine HCI, 70000-0080 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70000-0083 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 70000-0132 — Phenylephrine Hydrochloride, 70000-0133 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 70000-0141 — Guaifenesin, Phenylephrine HCl, 70000-0161 — Acetaminophen, Phenylephrine HCl, 70000-0191 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 70000-0192 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 70000-0211 — Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl, 70000-0223 — cocoa butter, phenylephrine HCl, +1566 more

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