FDA label 575dd7b5-2a34-d936-e063-6294a90a1078

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
2dcd1db5-8bf1-4296-b280-b4e2012e649c
SPL ID
575dd7b5-2a34-d936-e063-6294a90a1078
Version
2
Effective date
2026-07-24
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:29

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 avoid contact with the eyes or mucous membranes do not use on wounds or broken skin Stop use and ask a doctor if conditions worsen excessive skin irritation develops nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash occurs symptoms persists for more than 7 days If pregnant or breast-feeding , ask a doctor before use. 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.