ProCure 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
ProCure Antifungal Cream
Generic name
MICONAZOLE NITRATE 2%
Manufacturer
Twin Med LLC
Product type
HUMAN OTC DRUG
SPL set ID
39d55df5-8a8e-3a9b-e063-6294a90af20b
SPL ID
5828b30b-d1f1-9690-e063-6394a90ac037
Version
2
Effective date
2026-08-03
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:00:29
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.