FDA.reportPublic FDA data

FDA label 2f21d7f0-ac67-0cc5-e063-6294a90ace80

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
06eaf8b4-5a37-4056-be28-1504524e52de
SPL ID
2f21d7f0-ac67-0cc5-e063-6294a90ace80
Version
2
Effective date
2025-02-27
Source export date
2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:19:13

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

Warnnings For external use only. Do not use on children under 2 years of age except under the advice of a doctor. When using this product avoid contact with eyes. Stop use and ask a doctor if irritation occurs. there is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch). If pregnant or breast-feeding, ask a health professional before use Keep this and all drugs out of the reach of children. if swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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