FDA label 6bb668b8-a672-4dfb-e053-2991aa0a3ca5

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
ec58878f-ba74-486e-81c7-c90c6ddc4b9e
SPL ID
6bb668b8-a672-4dfb-e053-2991aa0a3ca5
Version
3
Effective date
2018-05-08
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:12

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) Discontinue using this product if symptoms listed below occurs. If conitued the condition may worsen. Speak to your dermatologist prior to resuming use. A) Rash, Red Spotting, Itchiness or edema occurs after use B) If applied area has symptoms as below when exposed to direct sunlight 2) Do not use on areas with wounds, skin irritations, eczma and on cracked skin. 3) Storage Instructions and Usage precautions A) Securely close the lid after use B) Keep out of reach of children C) Do not store in places of high or low temperature or expossed to direct sunlight.

Reported adverse events (FAERS/openFDA)#

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