WAXMAN KLEEN FREAK HAND SANITIZING WIPES- benzalkonium chloride cloth

WAXMAN KLEEN FREAK HAND SANITIZING WIPES by

Drug Labeling and Warnings

WAXMAN KLEEN FREAK HAND SANITIZING WIPES by is a Otc medication manufactured, distributed, or labeled by WAXMAN CONSUMER PRODUCTS GROUP INC., Zhejiang Ruolin Hygienic Products Co., Ltd., Guangzhou Daieme Cosmetic Cosmetic Co.,. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

Hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands thoroughly with product and allow to dry.
• Discard wipes in trash receptacle after use, Do not flush.
• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Propylene Glycol, Fragrance.

PRINCIPAL DISPLAY PANEL

Kills

99.9%

of Germs*

waxman

kleen

freak

hand sanitizing wipes

LEMON SCENT

clean and sanitize hands in one step

50 sheets

INGREDIENTS AND APPEARANCE

WAXMAN KLEEN FREAK HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80765-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80765-007-50	50 mL in 1 CANISTER; Type 0: Not a Combination Product	02/09/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/09/2021

Labeler - WAXMAN CONSUMER PRODUCTS GROUP INC. (877456673)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Ruolin Hygienic Products Co., Ltd.		415426870	manufacture(80765-007)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Daieme Cosmetic Cosmetic Co.,		542359812	manufacture(80765-007)