FDA label 79287139-1ac8-ca43-e053-2a91aa0a3f09

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
e4e00a64-1589-4a26-aa49-8b6facaeb64e
SPL ID
79287139-1ac8-ca43-e053-2a91aa0a3f09
Version
3
Effective date
2018-10-26
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 06:22:46

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 Do not use ■ in large quantities, particularly over raw surfaces or blistered areas. ■ on broken skin. ■ on irritated skin. When using this product ■ avoid contact with the eyes. ■ in case of contact, rinse off with water. Stop use and ask a doctor ■ condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. ■ irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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