FDA.reportPublic FDA data

FDA label 654946fc-51d0-47dc-a918-474e7ddfecf8

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
9b4ca28c-2998-4b4b-8a22-3936fcb0a110
SPL ID
654946fc-51d0-47dc-a918-474e7ddfecf8
Version
1
Effective date
2015-07-13
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 01:36:04

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 enternal use only Use only as directed. Avoid contact with eyes or mucus membranes. Discontinue use if excessive irritation of the skin developed. Do not bandage tightly, apply to wounds or damaged skin or use with a heating pad. If condition worsens, or if symptoms last more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. If 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.