# Docosanol

NDC: 51672-1406
Generic name: Docosanol
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20231026

FDA application: ANDA214454

## Active ingredients

- DOCOSANOL: 100 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1406"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1406
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5079b009-7f34-4d34-8f01-821365f04ca2