FDA label 05db0855-5e3c-38c8-e063-6294a90a2343

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
5bf11223-65a7-4b88-b9ae-80ec51d8e3e5
SPL ID
05db0855-5e3c-38c8-e063-6294a90a2343
Version
5
Effective date
2023-09-21
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:31:33

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 bandage tightly or use with aheating pad do not apply to wounds or damaged skin avoid contact with eyes or mucous membranes. Stop use and ask a doctor if condition worsens irritation develops redness is present symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breastfeeding ask a health professional prior to use. Keep out of reach of children. If swallowed, get medical help or contact Poison Control immediately.

Reported adverse events (FAERS/openFDA)#

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