ProCure Antifungal

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
ProCure Antifungal
Generic name
MICONAZOLE NITRATE 2%
Manufacturer
Twin Med LLC
Product type
HUMAN OTC DRUG
SPL set ID
3d375325-ddad-f1e1-e063-6394a90a679f
SPL ID
3d375325-ddae-f1e1-e063-6394a90a679f
Version
1
Effective date
2025-12-01
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:46:06
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Warnings For external use only Do not use Do not use on children under 2 years of age unless directed by a doctor When using this product When using this product avoid contact with eyes Stop using and ask a doctor if Stop using and ask a doctor if irritation occurs there is no improvement within 4 weeks (for athlete’s foot or ringworm) or 2 weeks (for jock itch) Keep out of reach of children Keep out of reach of Children . In case of accidental ingestion, contact a physician or Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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