FDA.reportPublic FDA data

FDA label 918142be-5081-4aa9-bbbe-51cf5aa25eae

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
56c85ec2-3416-41cf-af72-eaf3511842c3
SPL ID
918142be-5081-4aa9-bbbe-51cf5aa25eae
Version
3
Effective date
2013-09-03
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 06:13:15

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

For external use only. Not intended for pregnant, lactating women, or children under 2 years of age. Consult a doctor before use if you are taking prescription medication or have a serious medical condition. Do not apply to open wounds or get gel into eyes. If symptoms persist more than 7 days, or a rash or an allergic reaction develops, discontinue use and consult your physician. Do not use if allergic or sensitive to ingredients. Keep out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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