United States · FDA National Drug Code directory
Cold and Flu Daytime Severe
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
- 41250-643_ba58c7cb-227b-4bf4-a519-8cf4242bec41
- Product NDC
- 41250-643
- Form
- TABLET, FILM COATED
- Composition / generic term
- acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl
- Labeler
- Meijer Distribution Inc
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200508
- 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
- 2 BLISTER PACK in 1 CARTON (41250-643-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 41250-643-08
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 →