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
- 21922-023_a1fe87d9-27cf-4ff0-9e70-52b038882e36
- Product NDC
- 21922-023
- Form
- CREAM
- Composition / generic term
- Docosanol
- Labeler
- Encube Ethicals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221010
- Source listing expiry
- 20261231
Source-listed ingredients
- DOCOSANOL — 100 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PUMP in 1 PACKAGE (21922-023-17) / 2 g in 1 BOTTLE, PUMP · 21922-023-17
- 1 TUBE in 1 PACKAGE (21922-023-18) / 2 g in 1 TUBE · 21922-023-18
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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