United States · FDA National Drug Code directory
Tretinoin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 62032-413_cf3898ce-f8a0-4e8f-a237-a8d87e3c20a3
- Product NDC
- 62032-413
- Form
- GEL
- Composition / generic term
- Tretinoin
- Labeler
- Obagi Cosmeceuticals LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20140619
- Source listing expiry
- 20261231
Source-listed ingredients
- TRETINOIN — .05 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 20 g in 1 TUBE (62032-413-20) · 62032-413-20
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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