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
- 37808-603_d95ea6e4-b9ad-47ac-ab11-96cf09762808
- Product NDC
- 37808-603
- Form
- SOLUTION
- Composition / generic term
- acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
- Labeler
- H E B
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20160411
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 325 mg/15mL
- DEXTROMETHORPHAN HYDROBROMIDE — 10 mg/15mL
- GUAIFENESIN — 200 mg/15mL
- PHENYLEPHRINE HYDROCHLORIDE — 5 mg/15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 355 mL in 1 BOTTLE (37808-603-40) · 37808-603-40
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 →