Skip to main content

dg health night time cold and flu relief

NDC 55910-335 · Dolgencorp Inc

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine succinate
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL
Pharmacologic classAntihistamine [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]
Marketing categoryOTC MONOGRAPH DRUG

Packages

55910-335-34 — 237 mL in 1 BOTTLE (55910-335-34)

55910-335-40 — 355 mL in 1 BOTTLE (55910-335-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-135 — Acetaminophen, 55910-142 — acetaminophen, dextromethorphan hydrobromide, 55910-146 — Dextromethorphan HBr, Guaifenesin, 55910-149 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 55910-251 — Acetaminophen, 55910-272 — Dextromethorphan Hydrobromide / Guaifenesin, 55910-282 — Acetaminophen, 55910-297 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, 55910-300 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 55910-309 — Dextromethorphan HBr, 55910-336 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-345 — Acetaminophen, Aspirin, Caffeine, 55910-366 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 55910-374 — Acetaminophen, Aspirin, Caffeine, 55910-378 — Dextromethorphan HBr, Phenylephrine HCl, 55910-384 — dextromethorphan polistirex, 55910-398 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 55910-432 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-437 — Acetaminophen, Diphenhydramine HCl, 55910-440 — acetaminophen, aspirin, and caffeine, +4482 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels