2% MICONAZOLE NITRATE ANTIFUNGAL Cream

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
2% MICONAZOLE NITRATE ANTIFUNGAL Cream
Generic name
2% MICONAZOLE NITRATE ANTIFUNGAL CREAM
Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
56b54359-db21-b8b4-e063-6394a90a6f8c
SPL ID
56b54364-9b5d-b864-e063-6394a90aed25
Version
1
Effective date
2026-07-16
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:22
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Avoid contact with eyes. Do not use on children under 2 years of age unless directed by a doctor. Do not use for vaginal yeast infections. Ask a doctor before use if you have diabetes, immune system problems, or a condition covering more than half the affected area. Stop use and ask a doctor if irritation occurs, condition worsens, or there is no improvement within 2 weeks (jock itch) or 4 weeks (athlete's foot /ringworm). Keep out of reach of children. If swallowed, get medical help or contact Poison Control right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.