FDA.reportPublic FDA data

FDA label 9309836d-1381-21fe-e053-2995a90a6140

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
6296416a-6355-45e5-b2a5-c1e0ff2af57a
SPL ID
9309836d-1381-21fe-e053-2995a90a6140
Version
6
Effective date
2019-09-21
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:22:24

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For External Use only OTC -Do Not Use Section Do not use in the eyes ● Apply over a large areas of the body ● In case of deep puncture wounds, animal bites, or serious burns, consult a doctor. Other Required Warnings Do not use longer than 1 week unless directed by the doctor. OTC -Stop Use Section Stop use and consult a doctor if the condition persists or gets worse. Keep Out of Reach of Children Keep Out of Reach of Children

warnings

Other Required Warnings Do not use longer than 1 week unless directed by the doctor.

Reported adverse events (FAERS/openFDA)#

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