FDA label f267393d-4110-f400-e053-2995a90a7aa2

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
a0fdcd9d-74cc-4d80-8ac6-d479d6a2859f
SPL ID
f267393d-4110-f400-e053-2995a90a7aa2
Version
12
Effective date
2023-01-16
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:20:13

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 or mucous membranes do not apply to wounds or damaged skin do not use with other ointments, creams, sprays or liniments do not apply to irritated skin or if excessive irritation develops do not bandage wash hands after use with cool water do not use with heating pad or device store in a cool dry place Stop use and ask doctor if: condition worsens, or if symptoms persist for more than 7 days, or clear up and recur. If pregnant or breast feeding: ask a health professional befgore use.

Reported adverse events (FAERS/openFDA)#

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