United States · FDA National Drug Code directory
QCH Adult Tussin 541
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
- 83324-024_b487f4af-ad0c-4f18-9a6b-7fd386b3f46c
- Product NDC
- 83324-024
- Form
- LIQUID
- Composition / generic term
- Guaifenesin
- Labeler
- Chain Drug Marketing Association Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240502
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 200 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (83324-024-04) / 118 mL in 1 BOTTLE · 83324-024-04
Source and coverage
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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.
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