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
3d380fe4-a870-cb55-e063-6394a90a9c90
SPL ID
49758be2-d2d5-d4ad-e063-6294a90a9b03
Version
2
Effective date
2026-01-28
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:06:06
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.