FDA label 0756f58d-aac9-778c-e063-6294a90ae4f2

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
5bd3acd8-334d-4775-ab6a-7ac9f9dbc0c1
SPL ID
0756f58d-aac9-778c-e063-6294a90ae4f2
Version
4
Effective date
2023-10-10
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:29

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 When Using this product Use only as directed do not contact with the eyes or mucous membranes Do not bandage tightly. Do not use on wound, irritated or broken skin. Stop use and ask a doctor if Condition worsens. symptoms clear up and occur again within a few days. symptoms persist for more than 7 days. skin rash occurs or excessive irritation of the skin develops. If pregnant or breast feeding, ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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