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Green Guard Allergy 2 Relief

NDC 47682-017 · 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

47682-017-33 — 100 PACKET in 1 BOX (47682-017-33) / 2 TABLET, FILM COATED in 1 PACKET

47682-017-48 — 250 PACKET in 1 BOX (47682-017-48) / 2 TABLET, FILM COATED in 1 PACKET (47682-017-99)

47682-017-99 — 2 TABLET, FILM COATED in 1 PACKET (47682-017-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46122-418 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 46122-443 — Acetaminophen, Phenylephrine HCl, 46122-660 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 46122-677 — Mineral oil, Petrolatum, Phenylephrine, HCL, 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, 47682-047 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl , Guaifenesin, ,, 47682-108 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl ,, 47682-120 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, 47682-161 — 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, +1523 more

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