FDA label f42b2336-f911-6394-e053-2a95a90ac573

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
c8434954-3507-4851-9382-b1bf2c4442d3
SPL ID
f42b2336-f911-6394-e053-2a95a90ac573
Version
2
Effective date
2023-02-08
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:31:46

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 Do not use if you are allergic to any of the ingredients Ask a doctor before use if you have • Serious burns • Deep or puncture wounds • Animal bites When using this product • Do not use in the eyes • Do not apply over large areas of the body Stop use and ask a doctor if • You need to use more than 1 week • Condition persists or gets worse • Symptoms persist for more than 1 week or clear up and occur again within a few days. rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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