TATTOO NUMBING- lidocaine cream

Tattoo numbing by

Drug Labeling and Warnings

Tattoo numbing by is a Otc medication manufactured, distributed, or labeled by Guangzhou Sanshisan Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine:5%

INACTIVE INGREDIENT

Menthol
Chrysanthellum indicum extract
Portulaca oleracea extract
Vitamin E
Aloe Vera
Glycerin
Lecithin
Purified Water

PURPOSE

Local Anesthetic

WARNINGS

WARNING
For external use only.lf an allergic reaction occursdiscontinue use and consult adoctor.
lf pregnant or breastfeeding,consult a healthcare professionalbefore use.
Do not use if the seal is brokenor missing

STOP USE

Do not use if the seal is brokenor missing

DO NOT USE

lf pregnant or breastfeeding,consult a healthcare professionalbefore use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACHOF CHIDREN

If swallowed, go to the nearesthospital and seek immediatemedical help.

INDICATIONS & USAGE

USESTemporarily relieves localdiscomfort, itching, pain, soreness,or burning on the skin surface.

WHEN USING

WHEN USING THIS PRODUCTDo not exceed the recommended daily dosage unless directed bya doctor.
In case of accidental ingestionor overdose, seek medical helpimmediately or contact a PoisonControl Center.

DOSAGE & ADMINISTRATION

to an appropriate extent for product

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TATTOO NUMBING 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85342-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	3 g  in 60 g

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
PURSLANE (UNII: M6S840WXG5)
CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)
TOCOPHEROL (UNII: R0ZB2556P8)
AQUA (UNII: 059QF0KO0R)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85342-002-01	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	04/21/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/21/2025

Labeler - Guangzhou Sanshisan Cosmetics Co., Ltd. (699495407)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Sanshisan Cosmetics Co., Ltd.		699495407	label(85342-002) , manufacture(85342-002)