Medique Medi-Phenyl

NDC 47682-161 · Unifirst First Aid Corporation

Generic namePHENYLEPHRINE HYDROCHLORIDE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE

Strength5 mg/1

Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]

Marketing categoryOTC MONOGRAPH DRUG

Packages

47682-161-13 — 500 PACKET in 1 BOX (47682-161-13) / 2 TABLET, FILM COATED in 1 PACKET (47682-161-99)

47682-161-33 — 100 PACKET in 1 BOX (47682-161-33) / 2 TABLET, FILM COATED in 1 PACKET

47682-161-99 — 2 TABLET, FILM COATED in 1 PACKET (47682-161-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46122-689 — Phenylephrine hydrochloride, 46122-700 — Guaifenesin/phenylephrine, 46122-712 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 46122-776 — Hemorrhoidal, 46122-777 — Cocoa Butter, Phenylephrine HCl, 47682-001 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 47682-017 — PHENYLEPHRINE HYDROCHLORIDE, 47682-047 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl , Guaifenesin, ,, 47682-108 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl ,, 47682-120 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, 47682-162 — PHENYLEPHRINE HYDROCHLORIDE, 47682-435 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 47682-509 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 47682-543 — ACETAMINOPHEN,CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, 47682-735 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 47682-809 — PHENYLEPHRINE HYDROCHLORIDE, 47682-819 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 47682-835 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 47682-836 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 47682-919 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, +1523 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.