FDA.reportPublic FDA data

FDA label 0bf2f33a-af99-30a8-e063-6294a90a9349

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
0bf2ffa3-c87f-1297-e063-6394a90ab057
SPL ID
0bf2f33a-af99-30a8-e063-6294a90a9349
Version
1
Effective date
2023-12-07
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 06:05:48

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 When using this product ■ if following abnormal symptoms persist, discontinue use Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes ■ Stop immediately and consult a doctor if you experience 1) Hypersensitivity symptoms such as erythema, itching and dermatitis. 2) Skin Irritation 3) Following Instructions when using medication (1) For external use only (Do not use internally) (2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

Reported adverse events (FAERS/openFDA)#

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