FDA.reportPublic FDA data

FDA label 437fc6af-b61d-b18e-e063-6294a90a75b7

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)

SPL set ID
1dd8dd6c-23b7-4203-e063-6394a90affb6
SPL ID
437fc6af-b61d-b18e-e063-6294a90a75b7
Version
5
Effective date
2025-11-13
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:54:27

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 FOR EXTERNAL USE ONLY. Avoid contact with the eyes. Do not use on children under 2 years, unless directed by a doctor. Stop use and ask a doctor if irritation occurs there is no improvement within 4 weeks (for athlete’s foot and ringworm) or within 2 weeks (for jock itch) If pregnant or breast-feeding, consult a doctor before using this product. KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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