United States · FDA National Drug Code directory
Codeine-Guaifenesin
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
- 69367-272_82e575e8-9a6e-432e-8991-8f640de01dd6
- Product NDC
- 69367-272
- Form
- SOLUTION
- Composition / generic term
- Codeine Phosphate and Guaifenesin
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200715
- Source listing expiry
- 20261231
Source-listed ingredients
- CODEINE PHOSPHATE — 10 mg/5mL
- GUAIFENESIN — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 118 mL in 1 BOTTLE (69367-272-04) · 69367-272-04
- 473 mL in 1 BOTTLE (69367-272-16) · 69367-272-16
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 →