# Mucus Relief

NDC: 72090-011
Generic name: Guaifenesin
Labeler / Manufacturer: Pioneer Life Sciences, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20251222

FDA application: ANDA213420

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72090-011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72090-011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=be8ec612-41a8-479e-a889-7e09f2d27c10