FDA label ee0af5ab-e2fd-4415-a849-af88614743e2

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
63592010-08e3-4c02-9c73-95991b50af49
SPL ID
ee0af5ab-e2fd-4415-a849-af88614743e2
Version
3
Effective date
2020-11-25
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:34

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 Warnings: Flammable: keep away from flame or high heat. For external use only. Do not use the product on the following areas: around the eyes and ears, in the mouth, large body parts and damaged skin. Avoid contact with eyes. If contact occurs, wash with clean water and consult a doctor or pharmacist. If you experience any of the following symptoms, discontinue use of the product immediately and consult a physician or pharmacist: 1)Hypersensitivity symptoms(e.g. rash, erythema, itchiness, and edema), 2)Skin irritation symptoms. Keep out of reach of children. Replace cap after use.

Reported adverse events (FAERS/openFDA)#

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