# Mucus Relief Maximum Strength

NDC: 41520-732
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: 1200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"41520-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41520-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c94e3943-20da-4bd4-b0ff-6aa60b03a1bf