NUMIT- benzocaine, lidocaine hydrochloride, and tetracaine hydrochloride liquid 
Permanent Make Up Products LLC.

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Numit Liquid

ACTIVE INGREDIENTS

5.00% BENZOCAINE HYDROCHLORIDE, 2.00% LIDOCAINE HYDROCHLORIDE, 2.00% TETRACAINE HYDROCHLORIDE

INACTIVE INGREDIENTS

ETHYL ALCOHOL, PROPYLENE GLYCOL, AND TETRASODIUM EDTA

FOR EXTERNAL USE ONLY: For temporary relief of pain and swelling.

DIRECTIONS

Sensitivity test is strongly advised prior to use. Apply to area for temporary relief. Do not use more than 2 times a day. Store in a cool, dark place. Do not refrigerate.

WARNINGS

CLIENT EYE PROTECTANT SUGGESTED

Do not get in the mouth or eyes. Do not use product if you are pregnant or a nursing mother.

Keep out of the reach of children. If product comes into contact with the eyes wash immediatley. If accidentally swallowed seek immediate medical attention.

Do not use this product if you have any allergies to any of the product ingredients.

CAUTION

DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.

Distributed by
Permanent Make Up Products LLC.

PRINCIPAL DISPLAY PANEL - 14 G Bottle Label

NUMIT LIQUID

FOR PROFESSIONAL USE ONLY

1/2 FL OZ. (14G)

PMUP
PERMANENT
MAKE UP PRODUCTS

PRINCIPAL DISPLAY PANEL - 14 G Bottle Label
NUMIT 
benzocaine, lidocaine hydrochloride, and tetracaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84055-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine50 g  in 1000 g
Lidocaine Hydrochloride (UNII: V13007Z41A) (Lidocaine - UNII:98PI200987) Lidocaine Hydrochloride Anhydrous20 g  in 1000 g
Tetracaine Hydrochloride (UNII: 5NF5D4OPCI) (Tetracaine - UNII:0619F35CGV) Tetracaine Hydrochloride20 g  in 1000 g
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M) 500 g  in 1000 g
Propylene Glycol (UNII: 6DC9Q167V3)  
Edetate Sodium (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84055-009-011 in 1 BOX04/01/2024
114 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01704/01/2024
Labeler - Permanent Make Up Products LLC. (030421491)

Revised: 3/2024
Document Id: 63776565-0235-4f1b-b3f1-5e61c2133796
Set id: 674209b9-1dd4-443f-8c29-db6c5afa5a00
Version: 1
Effective Time: 20240312
 
Permanent Make Up Products LLC.