FDA.reportPublic FDA data

FDA label fce17636-1205-4408-bba0-4039a4266628

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
5d7f721a-9603-48bb-805a-c826fe901669
SPL ID
fce17636-1205-4408-bba0-4039a4266628
Version
3
Effective date
2021-10-28
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:25:28

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.  Keep out of reach of children.  In case of having side effects such as red rash, swollenness and/or itching while using the product, or in case such symptoms appear by direct sunlight after using it, consult a dermatologist immediately.  Do not apply the product on scar, eczema or dermatitis.  In contact with eyes rinse immediately with plenty of water  If not washed off with water after use, it may cause hair loss or discoloration.

Reported adverse events (FAERS/openFDA)#

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