FDA.reportPublic FDA data

FDA label 2a7ea170-a6a3-4dd2-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
9b8fc62a-3b6e-433f-a6d6-3c265ee1b799
SPL ID
2a7ea170-a6a3-4dd2-e054-00144ff8d46c
Version
2
Effective date
2016-01-29
Source export date
2026-08-01
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/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 22:59:52

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.