FUSION ANTIBACTERIAL WIPES- antibacterial wet wipes cloth

Fusion Antibacterial Wipes by

Drug Labeling and Warnings

Fusion Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Fusion Products Ltd., Hangzhou Lookon Commodity Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Antiseptic

Uses

For hand washing to decrease 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.

WHEN USING

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

Apply to clean dry hands.

Wet hands thoroughly with the product and allow to dry

Children under 6 should be supervised when using this product

Other information

Do not store above 104°F (40°C)

Do not use if seal is missing or broken

Inactive Ingredients

aloe barbadensis leaf juice, decyl glucoside, glycerin, water.

PRINCIPAL DISPLAY PANEL

70 WIPES, NDC: 80336-004-09

INGREDIENTS AND APPEARANCE

FUSION ANTIBACTERIAL WIPES 
antibacterial wet wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80336-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80336-004-09	70 in 1 BOTTLE; Type 0: Not a Combination Product	10/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/23/2020

Labeler - Fusion Products Ltd. (206910072)

Registrant - Hangzhou Lookon Commodity Co., Ltd. (541760483)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Lookon Commodity Co., Ltd.		541760483	manufacture(80336-004) , relabel(80336-004)