Skip to main content

Nighttime Cold and Flu Mini Softgels

NDC 83059-0129 · Shield Pharmaceuticals Corp

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 15; 6.25; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [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

83059-0129-1 — 1 BLISTER PACK in 1 CARTON (83059-0129-1) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

83059-0105 — Acetaminophen, Pyrilamine maleate, Caffeine, 83059-0106 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0107 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0112 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 83059-0113 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0114 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0116 — Dextromethorphan HBr, 83059-0119 — Acetaminophen, Pyrilamine maleate, Caffeine, 83059-0121 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0128 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0160 — Acetaminophen, 83059-0168 — Acetaminophen 500 mg, 83059-0170 — Dextromethorphan HBr, 83120-378 — LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE, 83311-335 — PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, 83324-017 — Acetaminophen, Caffeine, Pyrilamine maleate, 83324-023 — Dextromethorphan HBr, Guaifenesin, 83324-025 — Dextromethorphan HBr, Guaifenesin, 83324-026 — Dextromethorphan HBr, Guaifenesin, 83324-034 — Acetaminophen, +4930 more

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