FDA label e453096f-329f-c852-e053-2a95a90a2053

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
295a0386-dc05-4110-ba3d-0f040ba02543
SPL ID
e453096f-329f-c852-e053-2a95a90a2053
Version
2
Effective date
2022-07-21
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:26

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. Avoid contact with eyes. Do not use on children under 12 years of age unless directed by a doctor. When using this product some users may experience a mild skin irritation. Stop use and ask a doctor if skin irritation becomes severe. Keep out of the reach of children. If swallowed, seek medical help or contact a Poison Control Center right away. This product is not for use in the prevention of sunburn, Sun exposure should be limited by using a sunscreen agent: a sun blocking agent or protective clothing to cover bleached skin after treatment is completed to prevent darkening from reoccurring.

Reported adverse events (FAERS/openFDA)#

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