FDA label b34ce02d-9931-6700-e053-2a95a90ad4a6

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
6bab2757-5847-40a4-9980-121cc0cd7da2
SPL ID
b34ce02d-9931-6700-e053-2a95a90ad4a6
Version
2
Effective date
2020-11-04
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 02:06:54

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. Do not use on inflamed or brocken skin to prevent of sunburn if product is tan or brown When using this product mild irration may occur a avoid contact with eyes. If contact occurs, Rinse With water. avoid unnecessary sun exposure and use a sunscreen or protective clothing Stop use and ask a doctor if a gradual blue-black darkening of the skin occurs irritation becomes severe no improvement is seen after 3 months If pregnant or breast-feeding consult a health professional before use. Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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