United States · FDA National Drug Code directory

MUCUS RELIEF

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
72090-009_9f130a45-ac52-42e1-aff0-60eeb6492505
Product NDC
72090-009
Form
TABLET
Composition / generic term
guaifenesin 400 mg
Labeler
Pioneer Life Sciences, LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20240119
Source listing expiry
20261231

Source-listed ingredients

  • GUAIFENESIN — 400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 200 TABLET in 1 BOTTLE (72090-009-01) · 72090-009-01

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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