FDA label e9b8a309-86f9-852d-e053-2a95a90add1a

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
8cb94f1d-1e2e-531a-e053-2a95a90a1ba0
SPL ID
e9b8a309-86f9-852d-e053-2a95a90add1a
Version
4
Effective date
2022-09-28
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:59

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 More than one recommended dose at a time On broken or irritated skin If you are allergic to any ingredients of this product In large quantities, particularly over raw surfaces or blistered areas When using this product Use only as directed Avoid contact with eyes Do not wrap the treated skin with plastic wrap or other dressings or apply heat to the skin Stop use and ask a doctor if Condition worsens or symptoms persist for more than 7 days or clear up and occurs again Skin reactions occur, such as rash, itching, redness or irritation If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If product is 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.