FDA label 39b4d801-758a-4671-b063-300483ec09a0

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
966706bb-5574-4ed7-80d5-3115650bc6d3
SPL ID
39b4d801-758a-4671-b063-300483ec09a0
Version
1
Effective date
2012-05-29
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 01:42:38

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 . Keep out of reach of children. Do not apply heat, wrap or bandage to treated area. Avoid contact with eyes. Do not apply to open wound or irritated skin area. Do not use more than seven days continuously. Should contact with eyes occurs, rinse with cool water to remove. If pain does not go away or rash or irritation occurs, stop use and contact a physician.

Reported adverse events (FAERS/openFDA)#

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