FDA label 4e312560-6d2f-41bf-9a89-59b2c5b90cd8

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
660ef632-05b4-4358-9eb0-b6dc70f9746a
SPL ID
4e312560-6d2f-41bf-9a89-59b2c5b90cd8
Version
2
Effective date
2024-03-06
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:43:40

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 ■ If you experience any symptoms such as redness, swelling or itchiness during usage or from exposure to direct sunlight after usage, suspend use and consult a physician ■ Do not use on wounds or other areas of skin irritation ■ Keep out of reach of children ■ Keep away from direct sunlight

Reported adverse events (FAERS/openFDA)#

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