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XL-3 Day Time

NDC 76281-306 · AptaPharma Inc.

Generic nameACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 5 mg/15mL; mg/15mL; mg/15mL
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

76281-306-25 — 177 mL in 1 BOTTLE, PLASTIC (76281-306-25)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76162-792 — Acetaminophen, Chlorpheniramine Maleate, and Dextromethorphan Hydrobromide, 76162-811 — Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride, 76162-812 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 76162-912 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76162-913 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 76168-056 — Acetaminophen,Dextromethorphan,Doxylamine, 76168-119 — Acetaminophen PM, 76168-120 — Acetaminophen, 76281-304 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 76281-305 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 76281-307 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 76281-501 — ACETAMINOPHEN, 76281-502 — ACETAMINOPHEN, 76281-503 — DEXTROMETHORPHAN HYDROBROMIDE, 76281-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 76281-506 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76281-512 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 76281-515 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCl, 76281-517 — Dextromethorphan HBr, GUaifenesin, Phenylephrine HCL, 76281-519 — 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.