# Mucus Relief

NDC: 69256-731
Generic name: Guaifenesin
Labeler / Manufacturer: Harris Teeter, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230206
Marketing ended: 20261028
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:"69256-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69256-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7f2e64c-0fb9-413d-80ed-4d7cc2a07e0c