FDA label e1802c48-2690-4b7c-b211-2f9a05072b14

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
596ac9d9-28f6-4b9a-93cf-26c9afebac70
SPL ID
e1802c48-2690-4b7c-b211-2f9a05072b14
Version
1
Effective date
2018-01-22
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:41

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 ​When using this product • use only as directed • avoid contact with eyes, mucous membranes or rashes • do not apply to broken, wounded or damaged skin • do not bandage or cover with any type of wrap except clothing • do not use with a heating pad or apply external heat • discontinue use at least 1 hour before a bath or shower and do not use immediately after a bath or shower ​Stop use and ask a doctor if • rash, itching or excessive skin irritation develops • condition worsens or does not improve after regular use • symptoms persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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