FDA label 89c233f2-863e-4e96-9ad7-a24336422d87

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
56689533-7f1f-4259-afae-4748fd4ad6e8
SPL ID
89c233f2-863e-4e96-9ad7-a24336422d87
Version
1
Effective date
2012-06-01
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 01:35:37

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

For external use only When using this product Use only as directed do not bandage tightly or use with a heating pad avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin Stop use and ask doctor if Condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness is present irritation develops If pregnant or breast-feeding ask a health care professional before use. If swallowed, get medical help or contact a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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