FDA label 8bdd492a-0c1c-48d1-9aad-f30bb563bdab

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
681a046d-0d6f-46d8-a68d-9024f3be023a
SPL ID
8bdd492a-0c1c-48d1-9aad-f30bb563bdab
Version
3
Effective date
2014-08-20
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:00

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

For external use only. When using this product: Avoid application to wounded or infected area. DO NOT use if irritation develops. If so, consult a physician. Wash off immediately with cold water if product comes in contact with eyes. To avoide misuse, do NOT pour out the contents onto different container as doing so will affect product quality. Keep out of open flames. Store at a cool, dry place, away from direct sunlight.

Reported adverse events (FAERS/openFDA)#

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