FDA label 7207aaa1-1ea3-41c6-ad58-609063012405

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
160de12b-3f56-40c4-a048-3617567d2ab4
SPL ID
7207aaa1-1ea3-41c6-ad58-609063012405
Version
3
Effective date
2021-12-08
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:31:19

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. Avoid contact with eyes. If contact occurs, flush eyes with water immediately. Flammable Keep away from fire or flame. When using this product: Use only as directed Do not bandage or use with a heating pad Do not apply to wounds or damaged skin Discontinue use if irritation develops. Stop use and ask your doctor if: Condition worsens or if symptoms persist more than 7 days redness is present excessive irritation of the skin develops. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children, if ingested get medical help immediately.

Reported adverse events (FAERS/openFDA)#

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