FDA.reportPublic FDA data

FDA label 5e7e3c41-0fcb-4de9-b93b-e2c076c1a682

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
86fd2854-461a-4afc-8cdc-3e65c88d8a33
SPL ID
5e7e3c41-0fcb-4de9-b93b-e2c076c1a682
Version
10
Effective date
2020-04-17
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:12

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. For external use only. Avoid contact with the wound. Do not allow this product to come or nearby. If you accidentally touch a wound or eye, rinse immediately with water. If skin irritation or sensitivity occurs, discontinue use immediately and consult your doctor imediately. Not recommended for infants. Keep out of reach of children. Do not allow children under 6 years of age to handle or apply this product. If swallowed carelessly, contact your doctor immediately.

Reported adverse events (FAERS/openFDA)#

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