FDA label efcebaa1-ac47-4246-8a18-de877f734237

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
f709a23f-e22b-4490-b9b8-bbd29cf2dacd
SPL ID
efcebaa1-ac47-4246-8a18-de877f734237
Version
3
Effective date
2021-04-08
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:34:51

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 When using this product ● avoid contact with eyes and mucous membranes. ● do not apply to open wounds or damaged skin. ● make sure skin is clean and free of any creams ointments, sprays or liniments. ● do not cover with bandage. ● store in a cool, dry place. ● keep lid tightly closed. ● do not use with heating pads or heating devices. Discontinue use and consult a physician if skin irritation develops, condition recurs, worsens or symptoms persist for more than 7 days.

Reported adverse events (FAERS/openFDA)#

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