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NIGHTTIME CHERRY COLD AND FLU

NDC 21130-907 · BETTER LIVING BRANDS LLC.

Generic nameacetaminophen, dextromethorphan hydrobromide, and doxylamine succinate
Dosage formLIQUID
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

21130-907-02 — 2 BOTTLE in 1 PACKAGE (21130-907-02) / 354 mL in 1 BOTTLE (21130-907-01)

21130-907-06 — 236 mL in 1 BOTTLE (21130-907-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-707 — Dextromethorphan HBr, Guaifenesin, 21130-716 — Acetaminophen, Ibuprofen, 21130-719 — Acetaminophen, 21130-738 — Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl, 21130-746 — Acetaminophen, 21130-849 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 21130-866 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 21130-890 — Dextromethorphan polistirex, 21130-899 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 21130-900 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 21130-909 — Acetaminophen 650 mg, Dextromethorphan HBr 20 mg, Guaifenesin 400 mg, Phenylephrine HCl 10 mg, 21130-910 — Acteminophen, 21130-930 — Acetaminophen, Caffeine, Pyrilamine maleate, 21130-940 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 21130-945 — Acetaminophen, 21130-947 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine HCl, 21130-951 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 21130-986 — Doxylamine Succinate, 21130-989 — Guaifenesin and Dextromethorphan HBr, 21130-997 — Guaifenesin and Dextromethorphan HBr, +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