United States · FDA National Drug Code directory

Mucinex Fast-Max 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
63824-019_51b429cd-50ec-4059-e063-6294a90a40de
Product NDC
63824-019
Form
SOLUTION
Composition / generic term
dextromethorphan hydrobromide and guaifenesin
Labeler
Reckitt Benckiser LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20120718
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

  • 180 mL in 1 BOTTLE (63824-019-66) · 63824-019-66

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.

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Mucinex Fast-Max DM Max — United States | Molindra Medicines