United States · FDA National Drug Code directory

MUCUS RELIEF DM

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: 51316-858_39122e98-fa60-4363-b4af-9bdf196ea1ac
Product NDC: 51316-858
Form: TABLET, EXTENDED RELEASE
Composition / generic term: dextromethorphan hydrobromide, guaifenesin
Labeler: CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Marketing category: ANDA
Marketing start / end (source format): 20250714
Source listing expiry: 20271231

Source-listed ingredients

DEXTROMETHORPHAN HYDROBROMIDE — 30 mg/1
GUAIFENESIN — 600 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (51316-858-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE · 51316-858-01
1 BOTTLE in 1 CARTON (51316-858-78) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE · 51316-858-78

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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