# Retin-A

NDC: 0187-5172
Generic name: Tretinoin
Labeler / Manufacturer: Bausch Health US, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 19790730

FDA application: NDA017955

## Active ingredients

- TRETINOIN: .1 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0187-5172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0187-5172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9556d73d-c573-4e0a-9feb-764ce2d1107b