FDA label 2a6aa295-c4b9-0979-e054-00144ff8d46c

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
5a4eeb3f-ab3d-477c-86d6-f933affb20b4
SPL ID
2a6aa295-c4b9-0979-e054-00144ff8d46c
Version
5
Effective date
2016-01-28
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:19

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 and cautions

Warnings For external use only. Use only as directed. Avoid contact with eyes and mucous membranes. Do not apply to open wounds or damaged skin. Do not use in combination with any external heat source. Do not use on irritated or broken skin, or use in combination with any bandage, wrap, stocking or similar device or garment. Consult physician for children under 12 years of age. Do not use if allergic to Camphor, Histamine, Menthol or any other components. Stop use and consult physician if symptoms worsen or persist for more than 7 days. Stop use if itching or excessive skin irritation occurs. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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