FDA label 89e4716e-3682-41a5-9e3d-454c3c33f8f0

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
4cbebf3f-0752-4e18-89ea-4f0f518ed07b
SPL ID
89e4716e-3682-41a5-9e3d-454c3c33f8f0
Version
1
Effective date
2018-04-23
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 01:26:29

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. Avoid contact with eyes and mucus membranes. It can take 1 to 2 weeks before therapeutics effect is felt. For use beyond 6 weeks, consult a health care practitioner Do not Apply to wounds or damaged skin. Bandage tightly. Inhale. Apply with external heat, such as an electric pad, as this may result in excessive skin irritation or skin burn. When using this product Use only as directed. Keep out of reach of children. If overdose or accidental ingestion occurs, call a poison control center immediately. Consult a healthcare practitioner prior to use if you are pregnant or breastfeeding. Stop use and ask a doctor if you experience hypersensitivity, rashes and/or burning discomfort, headache or redness or if symptoms worsen or re-occur with a few days.

Reported adverse events (FAERS/openFDA)#

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