WET WIPES- benzethonium chloride swab 
Kareway Product, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Pure-Aid Wet Wipes

Active Ingredients

Benzethonium Chloride 0.3%

Purpose

Antibacterial

Use

decrease bacteria on skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients

When using this product

do not get into eyes. If contact occurs, rinse throroughly with water.

Stop use and ask a doctor

if irritation or rash develops and continues for more than 72 hours

Keep out of reach of children

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

Directions

adults and children 2 years and over

Children under 2 years

Inactive Ingredients

Water, Butylene Glycol, Alcohol, Hyaluronic Acid, Polysorbate 80, Sodium Lauryl Sulfate, Disodium Lareth Sulfosuccinate,

Glycerin, Phytosqualane, Anthemis Nobilis Flower Extract, Camellia Sinensis Leaf Extract, Cyclopia Intermedia Leaf Extract,

Tocopheryl Acetate, Phenoxyethanol, Disodium EDTA, Fragrance

Principle Display Panel

Fresh Scent

Wet wiptes

Antibacterial formula

30 wipes

wipes

WET WIPES 
benzethonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67510-0888
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.3   in 100 
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
HYALURONIC ACID (UNII: S270N0TRQY)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
GLYCERIN (UNII: PDC6A3C0OX)  
CYCLOPIA INTERMEDIA LEAF (UNII: 29UXG2GG8O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67510-0888-330 in 1 POUCH; Type 0: Not a Combination Product06/30/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/30/2015
Labeler - Kareway Product, Inc. (121840057)

Revised: 7/2020
Document Id: ab9c666a-09f0-629f-e053-2995a90ab96a
Set id: 19c5a7a3-d381-6f73-e054-00144ff8d46c
Version: 2
Effective Time: 20200729
 
Kareway Product, Inc.