Active Ingredients
LIDOCAINE 5%
Hilook Blue Gel Anesthetic Gel
FDA Label NDC 83566-143
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Aimu Biological Technology Co., Ltd for the product Hilook Blue Gel Anesthetic (NDC 83566-143). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, stop use and ask a doctor if, do not use, when using this product, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
lieduce pain and swelling during tattouermanent cosmetics,electrolysis other pain sensitive procedures
Uses
After cleaning the skin, apply an appropriate amount of gel to the area to be treated.
Massage gently for a few minutes and wait for 15 to 30 minutes for the gel to take effect as an anesthetic.
Warnings
For external use only.
Stop Use And Ask A Doctor If
rash occurs.
Do Not Use
on damaged or broken skin.
When Using This Product
keep out of eyes. Rinse with water to remove.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage
Squeeze out an appropriate amount of product and spread evenly on skin.
Inactive Ingredients
WATER 36.7%
ALCOHOL 15%
POLYSORBATE 20 3%
GLYCERIN 20%
PROPYLENE GLYCOL 10%
YUCCA GLAUCA ROOT EXTRACT 2%
ACHILLEA MILLEFOLIUM FLOWER EXTRACT 3%
CAPRYLYL GLYCOL 0.3%
DISODIUM EDTA 0.2%
PHENOXYETHA-NOL 0.3%
CARBOMER 3.5%
TRIETHANOLAMINE 1%
Package Label.Principal Display Panel
Label (01)
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