# Mucus Relief

NDC: 41163-731
Generic name: Guaifenesin
Labeler / Manufacturer: United Natural Foods, Inc. dba UNFI
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180930

FDA application: ANDA207342

## 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:"41163-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41163-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7d457a6-05f9-407c-bf9b-a82e3cf2568c