FDA.reportPublic FDA data

FDA label 4470ed81-4c10-ba4d-e063-6294a90ad130

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
776ca76a-a6cc-5238-e053-2a91aa0abfcb
SPL ID
4470ed81-4c10-ba4d-e063-6294a90ad130
Version
10
Effective date
2025-11-25
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:29:49

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 Do not use on children under 2 years of age unless directed by a doctor for diaper rash When using this product avoid contact with the eyes Stop use and ask a doctor if irritation occurs there is no improvement within 2 weeks when used for the treatment of jock itch there is no improvement within 4 weeks when used for athlete's foot or ringworm If swallowed, get medical help or contact a Poison Control Center (1800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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