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Nasal Decongestant PE

NDC 37835-651 · Bi-Mart

Generic namePHENYLEPHRINE HYDROCHLORIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

37835-651-01 — 100 TABLET in 1 BOTTLE (37835-651-01)

37835-651-36 — 36 TABLET in 1 BOTTLE (37835-651-36)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 37808-775 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-811 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 37808-848 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37808-864 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37808-987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 37808-994 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37835-520 — acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 37835-526 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 37835-527 — acetaminophen, dextromethorphan HBr, Phenylephrine HCl, 41163-035 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-047 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-053 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-158 — Ibuprofen, phenylephrine HCl, 41163-188 — mineral oil, petrolatum, phenylephrine HCl, 41163-279 — cocoa butter, phenylephrine HCl, 41163-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 41163-648 — Phenylephrine hydrochloride, 41163-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, +1522 more

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