United States · FDA National Drug Code directory
Desenex
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
- 0316-0225_4833f384-eb1d-0049-e063-6394a90a9f53
- Product NDC
- 0316-0225
- Form
- POWDER
- Composition / generic term
- MICONAZOLE NITRATE
- Labeler
- Crown Laboratories
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20231019
- Source listing expiry
- 20271231
Source-listed ingredients
- MICONAZOLE NITRATE — 20 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 43 g in 1 BOTTLE, PLASTIC (0316-0225-01) · 0316-0225-01
- 85 g in 1 BOTTLE, PLASTIC (0316-0225-02) · 0316-0225-02
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 →