FDA.reportPublic FDA data

FDA label 937d0439-12a8-4f57-943e-3f5f9926463e

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
d7ea3cfc-dc14-4039-ac6b-7176dbe70cf5
SPL ID
937d0439-12a8-4f57-943e-3f5f9926463e
Version
2
Effective date
2016-11-04
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 02:47:53

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 • do not get into eyes or on mucous membranes • do not apply to wounds or to damaged or very sensitive skin • do not bandage tightly or cover with any type of wrap except clothing • do not bandage tightly Stop use and ask a doctor if • condition worsens • excessive irritation, burning or discomfort of the skin develops • 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.