FDA label 365809e7-0dd2-132f-e063-6394a90a3e76

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
0fc01581-39d0-7a8b-e063-6394a90a478f
SPL ID
365809e7-0dd2-132f-e063-6394a90a3e76
Version
2
Effective date
2025-05-30
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 05:12:40

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 * Do not use the product on children under 10 years ofage unless directed by a doctor. *Forexternal use only. if swallowed, seek immediatemedical assistance. *Safeguard the product from children to avert anychance of accidentalingestion..lmmediate discontinuation is advised in case of discomfort or irritation. * Refrain from applying the product on injured orswollen skin areas. *Forindividuals with sensitive skin, a patch test on thewrist's interior isrecommended before use,ensuring anirritation-free experience. *Keep the product away from the eyes to preventcontact.

Reported adverse events (FAERS/openFDA)#

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