FDA label 1859ab3f-5eef-49a5-aa22-4af3c266ece0

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
db6dfd0d-930b-4322-bf6e-a130bde52169
SPL ID
1859ab3f-5eef-49a5-aa22-4af3c266ece0
Version
3
Effective date
2022-09-08
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:32

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 -------------------------------------------------------------------------------------------------------- Stop use and ask a doctor if ■ hypersensitivity, skin irritation, or rash develops and persists -------------------------------------------------------------------------------------------------------- Do not use ■ in combination with soap or antibacterial cleansing agents -------------------------------------------------------------------------------------------------------- When using this product ■ avoid using repeatedly in the same area as skin irritation may occur ■ avoid getting into the eyes (if contact occurs, wash well with clean water) ■ if the following abnormal symptoms persist (irritation around the eyes, ears, mucous membranes, including the mouth, and skin rashes), discontinue use

Reported adverse events (FAERS/openFDA)#

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