FDA label 3a805223-101e-4b49-9a6f-a77b127d5d51

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
b831463d-1c7d-44e1-9b8c-f03d31e15829
SPL ID
3a805223-101e-4b49-9a6f-a77b127d5d51
Version
1
Effective date
2010-08-28
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:51

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. Do not bandage tightly. Do not apply heat to the area of application. Do not apply to open wounds or damaged skin. Avoid contact with eyes or mucous membranes. Ask a doctor before use, if you have ever experienced a reaction due to ingredients listed. Stop use and consult a licensed health professional if conditions worsens or if symptoms persists for more than 7 days, or clears up and occurs again. If pregnant or breast feeding, ask the health professional before use. Keep out of reach of children. If ingestion occurs, 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.