FDA label 6a76c93a-8088-43b2-a340-16aa6bb4cb5f

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
38eb19ae-a170-4588-b7a5-1c14b401ac3e
SPL ID
6a76c93a-8088-43b2-a340-16aa6bb4cb5f
Version
3
Effective date
2018-03-29
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:24

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 Ask a doctor before use • On children under 2 years of age 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 and ringworm) or 2 weeks (for jock itch)

Reported adverse events (FAERS/openFDA)#

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