United States · FDA National Drug Code directory

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
49035-930_2d52873a-2297-46c8-bf87-72afade1592c
Product NDC
49035-930
Form
SOLUTION
Composition / generic term
Dextromethorphan HBr, Guaifenesin
Labeler
Wal-Mart Stores Inc
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20180815
Source listing expiry
20271231

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, PLASTIC in 1 CARTON (49035-930-19) / 237 mL in 1 BOTTLE, PLASTIC (49035-930-00) · 49035-930-19

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 →