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Severe Sinus Congestion and Pain

NDC 83059-0107 · Shield Pharmaceuticals Corp

Generic nameAcetaminophen, Guaifenesin, Phenylephrine
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 200; 5 mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

83059-0107-1 — 1 BLISTER PACK in 1 CARTON (83059-0107-1) / 12 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

83059-0023 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0024 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 83059-0044 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0045 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0052 — Acetaminophen, Guaifenesin, 83059-0057 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0071 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0103 — Acetaminophen, 83059-0105 — Acetaminophen, Pyrilamine maleate, Caffeine, 83059-0106 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0112 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 83059-0113 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0114 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0119 — Acetaminophen, Pyrilamine maleate, Caffeine, 83059-0121 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0128 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0129 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 83059-0160 — Acetaminophen, 83059-0168 — Acetaminophen 500 mg, 83120-378 — LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE, +4982 more

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