FDA label 1ac45dcf-6101-1a8b-e054-00144ff8d46c

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
1ac45dcf-6100-1a8b-e054-00144ff8d46c
SPL ID
1ac45dcf-6101-1a8b-e054-00144ff8d46c
Version
1
Effective date
2015-07-13
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:41:43

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

WARNINGS FOR EXTERNAL USE ONLY. When using this product use only as directed Do not bandage tightly Do not use with a heating pad Agoid contact with the eyes or mucous membranes Do not apply to wounds or damaged or irritated skin

warnings and cautions

STOP USE AND ASK A DOCTOR IF Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days Redness is present Irritation develops

Reported adverse events (FAERS/openFDA)#

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