NPAG TATTOO NUMBING CREAM cream

NPAG Tattoo Numbing Cream by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient(s)

Procaine 5%

Tetracaine 1%

Prilocaine 1%

Purpose

Topical anesthetic

Use

Tattoo, waxing and hair removal etc.

Warnings

For external use only.

Do not use

on open skin wounds. in or near the eyes. In case of contact, rinse eyes
thoroughly with water and stop using.

WHEN USING

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes
thoroughly with water.

STOP USE

and ask a doctor if irritation or rash occurs. These may be signs of allergy.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison C ontrol Center right
away.

Directions

After cleaning the skin [warm water is better), apply appropriate amount of
tattoo cream to the area to be tattooed, cover the plastic wrap,
Wait 50 mins to 60 mins for the numbing cream to take effect,
then get tattooed.

Other information

No data available

Inactive ingredients

Water, Propylene Glycol, Carbomer, Glycerin, Disodium Edta,
Hydroxyacetophenone, 1 ,2- Hexanediol, Mentha Arvensis Leaf
Extract, Chrysanthellum Indicum Extract, Portulaca Oleracea Extract,
Peg- 40 Hydrogenated Castor.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

NPAG TATTOO NUMBING CREAM 
npag tattoo numbing cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84353-001
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROCAINE (UNII: 4Z8Y51M438) (PROCAINE - UNII:4Z8Y51M438)	PROCAINE	5 g  in 100 mL
TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV)	TETRACAINE	1 g  in 100 mL
PRILOCAINE HYDROCHLORIDE (UNII: MJW015BAPH) (PRILOCAINE - UNII:046O35D44R)	PRILOCAINE HYDROCHLORIDE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84353-001-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/24/2024

Labeler - USA MINGER Inc. (123952552)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(84353-001)

Establishment
Name	Address	ID/FEI	Business Operations
USA MINGER Inc		123952552	label(84353-001)