United States · FDA National Drug Code directory
MICONAZOLE Nitrate 2%
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
- 71399-0071_b1ef7656-ad4c-4c56-987a-18628f9d9dca
- Product NDC
- 71399-0071
- Form
- CREAM
- Composition / generic term
- MICONAZOLE NITRATE
- Labeler
- Akron Pharma Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20241119
- Source listing expiry
- 20261231
Source-listed ingredients
- MICONAZOLE NITRATE — 2 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 BOX (71399-0071-1) / 14.2 g in 1 TUBE · 71399-0071-1
- 1 TUBE in 1 BOX (71399-0071-3) / 28.4 g in 1 TUBE · 71399-0071-3
- 1 TUBE in 1 BOX (71399-0071-4) / 42.5 g in 1 TUBE · 71399-0071-4
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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