FDA.reportPublic FDA data

FDA label c941a010-1597-490d-9014-cd09d0d7171b

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
6e3e2926-f2c4-43da-8096-abb7e951a020
SPL ID
c941a010-1597-490d-9014-cd09d0d7171b
Version
1
Effective date
2019-05-08
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:09

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 1. Discontinue use if the following signs of irritation develop during using the cosmetics, and consult your dermatologist. If you keep using, it will aggravate the symptoms. 1) Rashes, swell, itching, or irritation during using 2) Such irritations as above in the applied spot due to an exposure to direct sunlight 2. Do not apply in the area of cut, eczema, or dermatitis. 3. Warning 1) Keep out of reach of children. 2) Keep out of places exposed to the direct sunlight and too hot or too cold places.

Reported adverse events (FAERS/openFDA)#

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