FDA.reportPublic FDA data

FDA label 25846d7a-0625-6792-e063-6394a90ae8f5

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
25847463-6d6b-202f-e063-6294a90a6c37
SPL ID
25846d7a-0625-6792-e063-6394a90ae8f5
Version
1
Effective date
2024-10-27
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:03:45

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

1.Avoid accidentally entering the eyes.If accidentally entering the eyes,immediately rinse with plenty of water. 2.Everyone has different skin characteristics.If you feel uncomfortable or have abnormal skin reactions during use,please stop orconsult a dermatologist 3.Please keep out of reach of infants and young children,and seal promptly after use. 4.Contains salicylic acid;Do not use for children under three years old. 5. Use together with sunscreen cosmetics. 6.Do not swallov.

Reported adverse events (FAERS/openFDA)#

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