WET WIPES- benzethonium chloride swab

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Kareway Product, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• apply to hands
• allow to dry without wiping

Children under 2 years

• ask a doctor before use

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

INGREDIENTS AND APPEARANCE

WET WIPES 
benzethonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67510-0888
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.3   in 100

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67510-0888-3	30 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/30/2015

Labeler - Kareway Product, Inc. (121840057)