FDA label 7427b1f5-0faa-4e31-aa91-893d57f78851

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
a14267e0-d42e-4ce9-b4b0-e71d4223f3e0
SPL ID
7427b1f5-0faa-4e31-aa91-893d57f78851
Version
2
Effective date
2022-01-24
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:43:27

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 if skin is irritated or damaged excessive irritation develops 12 years of age or under When using this product avoid contact with the eyes and mucous membranes do not apply to wounds, damaged, broke or irrated skin do not bandage tightly or use a heating pad do not swallow If swallowed, contact a physician or contact a poison control center immediately Stop and ask doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness develops If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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