United States · FDA National Drug Code directory

daytime severe cold and flu

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51316-731_78756f2c-939b-46fc-b34f-f2d2b823be96
Product NDC
51316-731
Form
TABLET, FILM COATED
Composition / generic term
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20260407
Source listing expiry
20271231

Source-listed ingredients

  • ACETAMINOPHEN — 325 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE — 10 mg/1
  • GUAIFENESIN — 200 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 BLISTER PACK in 1 CARTON (51316-731-62) / 2 TABLET, FILM COATED in 1 BLISTER PACK · 51316-731-62

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →