# Mucus Relief Extended Release

NDC: 41520-731
Generic name: Guaifenesin
Labeler / Manufacturer: Care One (American Sales Company)
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181231

FDA application: ANDA207342

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"41520-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41520-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96569c70-0936-4041-ab32-2b2262402f34