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foster and thrive daytime cold and flu relief

NDC 70677-1031 · Strategic Sourcing Services LLC

Generic nameacetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 5 mg/15mL; mg/15mL; mg/15mL
Pharmacologic classAdrenergic alpha1-Agonists [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

70677-1031-1 — 237 mL in 1 BOTTLE (70677-1031-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-0101 — Brompheniramine maleate, Phenylephrine HCl, 70677-0117 — Acetaminophen, 70677-0121 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 70677-1004 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1005 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1025 — dextromethorphan polistirex, 70677-1026 — dextromethorphan polistirex, 70677-1027 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1029 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1030 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 70677-1032 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70677-1033 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 70677-1035 — dextromethorphan hydrobromide, guaifenesin, 70677-1036 — Dextromethorphan HBr, Guaifenesin, 70677-1049 — Guaifenesin, Dextromethorphan HBr, 70677-1050 — Guaifenesin, Dextromethorphan HBr, 70677-1055 — Dextromethorphan Hydrobromide / Guaifenesin, 70677-1056 — Guaifenesin/phenylephrine, 70677-1108 — mineral oil, petrolatum, phenylephrine HCl, 70677-1119 — Acetaminophen, +4867 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