FDA label 526a0f29-a5bf-cea2-e063-6294a90a98f3

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
c9e3cc96-43b1-411e-a394-45598e7b4731
SPL ID
526a0f29-a5bf-cea2-e063-6294a90a98f3
Version
10
Effective date
2026-05-22
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:20

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 Do not use on children under 2 years of age unless directed by a doctor. For external use only. Avoid contact with eyes. Stop use and ask a doctor if irritation occurs there is no improvement within 4 weeks for athlete's foot and ringworm or 2 weeks for jock itch If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Reported adverse events (FAERS/openFDA)#

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