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
- 72090-012_022e6fd9-1e64-4364-a117-67354fed2fa0
- Product NDC
- 72090-012
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin
- Labeler
- Pioneer Life Sciences, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251204
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 1200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-01) · 72090-012-01
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-02) · 72090-012-02
- 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-03) · 72090-012-03
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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