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Allergy Multi Symptom

NDC 37808-628 · HEB

Generic nameACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 2; 5 mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

37808-628-02 — 2 BLISTER PACK in 1 CARTON (37808-628-02) / 12 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 37808-466 — Acetaminophen, Phenylephrine Hydrochloride, 37808-482 — Acetaminophen, 37808-497 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-499 — Acetaminophen, 37808-556 — Acetaminophen, Diphenhydramine HCl, 37808-574 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-586 — Acetaminophen, Aspirin, Caffeine, 37808-598 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 37808-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 37808-663 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-704 — Acetaminophen, 37808-718 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 37808-728 — Phenylephrine hydrochloride, 37808-747 — Acetaminophen, 37808-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 37808-768 — Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate, 37808-775 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-792 — Acetaminophen, +4226 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels