FDA label 6bd12a64-9929-42e9-8cb8-d8043b1f3d66

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
907784e5-cec1-4eb0-b9df-87f9891f0ad6
SPL ID
6bd12a64-9929-42e9-8cb8-d8043b1f3d66
Version
1
Effective date
2015-05-05
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 05:13:33

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

Warning - For external use only. In case of accidental ingestion, get help or contact a poison control center immediately. Do not use on irritated skin in or near eyes or mucous membranes on wounds or damaged skin if prone to allergic reaction from any ingredient on large area of the body Ask a doctor or pharmacist before use if you are taking any other medication or drinking alcohol. Stop use and ask a doctor if condition worsens or clears up and occurs again, if symptoms persist for more than 7 days or irritation or severe burning occurs. If pregnant or breast-feeding ask a health professional before use. Keep at room temperature.

Reported adverse events (FAERS/openFDA)#

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