United States · FDA National Drug Code directory
DOCOSANOL
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
- 0713-0353_e4d903b2-6585-4e80-a58e-128fe69cf1d4
- Product NDC
- 0713-0353
- Form
- CREAM
- Composition / generic term
- Docosanol
- Labeler
- Cosette Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240104
- Source listing expiry
- 20261231
Source-listed ingredients
- DOCOSANOL — 100 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (0713-0353-02) / 2 g in 1 TUBE · 0713-0353-02
- 1 BOTTLE, PUMP in 1 CARTON (0713-0353-62) / 2 g in 1 BOTTLE, PUMP · 0713-0353-62
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →