FDA label bb7f3c11-acfb-4b01-829d-20d77054b54a

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
cf85b8db-ba3c-4478-9456-90d7adb65286
SPL ID
bb7f3c11-acfb-4b01-829d-20d77054b54a
Version
2
Effective date
2017-12-27
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:14

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. If you are taking any prescription medication or have a serious medical condition, ask a doctor before use. Do not bandage tightly or apply to wounds or damaged skin. Do not get gel into eyes. If condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days, or if a rash or an allergic reaction develops, stop use and consult your physician. Keep out of the reach of children. Not for pregnant or lactating women, or children under 14. Do not apply over large areas of the body. Not for use by persons with allergic sensitivities to Arnica nor any other ingredient.

Reported adverse events (FAERS/openFDA)#

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