HILOOK NUMBING CREAM- lidocaine cream

Hilook Numbing Cream by

Drug Labeling and Warnings

Hilook Numbing Cream by is a Otc medication manufactured, distributed, or labeled by Guangdong Aimu Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

LIDOCAINE 5%
TETRACAINE 1%
PRILOCAINE 1%

Purpose

Deep numbness fast and painless

Uses

After cleaning the skin(warm water is better), apply appropriate amount of tattoo cream to the area to be tattooed, wrap the plastic wrap,.

Wait 40 minutes to an hour for the numbing cream to take effect.

And then get tattooed.

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 51.8%
PROPYLENE GLYCOL 10%
CARBOMER 3%
GLYCERIN 15%
DISODIUM EDTA 0.2%
HYDROXYACETOPHENONE 1.5%
1,2-HEXANEDIOL 1.5%
MENTHAARVENSIS LEAF EXTRACT 2%
CHRYSANTHELLUM INDICUM EXTRACT 2%
PORTULACA OLERACEA EXTRACT 3%
PEG-40 HYDROGENATED CASTOR 3

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HILOOK NUMBING CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-142
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV)	TETRACAINE	1 g  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 mL
PRILOCAINE (UNII: 046O35D44R) (PRILOCAINE - UNII:046O35D44R)	PRILOCAINE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-142-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/24/2024

Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(83566-142)