United States · FDA National Drug Code directory
equate adult tussin dm max
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
- 49035-705_695fbdf9-b90d-4a7e-bd93-b38e55e8e78b
- Product NDC
- 49035-705
- Form
- SOLUTION
- Composition / generic term
- Dextromethorphan HBr, Guaifenesin
- Labeler
- Wal-Mart Stores Inc
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20181002
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 20 mg/20mL
- GUAIFENESIN — 400 mg/20mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (49035-705-26) / 118 mL in 1 BOTTLE · 49035-705-26
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 →