FDA label 29b34f15-4374-4517-871e-c356dc79578e

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
04c3daac-f2f4-4ccd-a4b5-16899767301d
SPL ID
29b34f15-4374-4517-871e-c356dc79578e
Version
1
Effective date
2016-10-24
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:51

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 Warnings: 1. Stop using the product if the following problems arise while using the product as continued use could worsen the symptoms; consult with a dermatologist. 2. Do not use on areas with wounds, eczema, and dermatitis. 3. Storage and handling precautions. 4. Wash off the product if it gets in the eye. 5. Inadequate cleansing after use could lead to bleaching; cleanse adequately after use. 6. Keep out of reach of children. 7. Store in a cool, dry place away from direct sunlight. 8. External use only.

Reported adverse events (FAERS/openFDA)#

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