United States · FDA National Drug Code directory
Desonide
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
- 72162-2005_a0792f7b-faeb-475d-a030-ef46e876c2d0
- Product NDC
- 72162-2005
- Form
- CREAM
- Composition / generic term
- Desonide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200617
- Source listing expiry
- 20271231
Source-listed ingredients
- DESONIDE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (72162-2005-2) / 15 g in 1 TUBE · 72162-2005-2
- 1 TUBE in 1 CARTON (72162-2005-6) / 60 g in 1 TUBE · 72162-2005-6
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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