Skip to main content

Theraflu Severe Cold Relief Daytime Berry Burst

NDC 0067-6800 · Haleon US Holdings LLC

Generic nameAcetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride
Dosage formPOWDER
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength650; 20; 10 mg/1; mg/1; mg/1
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

0067-6800-02 — 6 POWDER in 1 CARTON (0067-6800-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0067-2035 — Acetaminophen, Asprin, Caffeine, 0067-2039 — Acetaminophen, Aspirin (NSAID) and Caffeine, 0067-2040 — Acetaminophen, Aspirin, and Caffeine, 0067-2042 — Acetaminophen, Aspirin (NSAID), Caffeine, 0067-2056 — Acetaminophen, Aspirin (NSAID) and Diphenhydramine Citrate, 0067-2086 — Phenylephrine hydrochloride, 0067-2200 — acetaminophen, 0067-6094 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE, 0067-6095 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 0067-6426 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0067-6801 — Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride, 0067-6802 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0067-6803 — ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl, 0067-7917 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE, 0067-7918 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 0067-7921 — Acetaminophen, Dextromethorphan HBr, 0067-7922 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 0067-8127 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0067-8129 — Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl, 0067-8132 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +4867 more

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