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Good Sense Severe Daytime Cold and Flu

NDC 0113-0603 · L. Perrigo Company

Generic nameacetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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

0113-0603-34 — 237 mL in 1 BOTTLE (0113-0603-34)

0113-0603-40 — 354 mL in 1 BOTTLE (0113-0603-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-0212 — Acetaminophen, 0113-0279 — cocoa butter, phenylephrine HCl, 0113-0335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0374 — Acetaminophen, Aspirin, Caffeine, 0113-0384 — dextromethorphan polistirex, 0113-0403 — Acetaminophen, 0113-0437 — Acetaminophen, Diphenhydramine HCl, 0113-0459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0484 — Acetaminophen, 0113-0544 — Acetaminophen, 0113-0608 — Acetaminophen, 0113-0648 — Phenylephrine hydrochloride, 0113-0656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 0113-0763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 0113-0812 — dextromethorphan HBr, guaifenesin, 0113-0927 — Dextromethorphan HBr, Guaifenesin, 0113-0944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 0113-0946 — Acetaminophen, 0113-0958 — dextromethorphan polistirex, 0113-0987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, +5267 more

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