WIPE OUT SAFE PACK- alcohol, benzalkonium chloride kit

WIPE OUT Safe Pack by

Drug Labeling and Warnings

WIPE OUT Safe Pack by is a Otc medication manufactured, distributed, or labeled by TZUMI INNOVATIONS LLC, Shenzhen Meiya Display Co., Ltd., Shenzhen Lantern Science Co., ltd., FuYang YangYang Health Technology Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WIPE OUT Hand Sanitizer with Moisturizers

WIPE OUT Hand Sanitizer with Moisturizers

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

■ To decrease bacteria on the skin

WARNINGS

For external use only

Flammable. Keep away from fire or flame

When using this product, avoid contact with eyes
If contact occurs, rinse eyes thoroughly with water

Stop Use

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours

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

Take a palmful of product in one hand, spread on both hands and rub into skin

Other information

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

Water, Glycerin, Aloe Barbadensis Leaf Extract, AMINOMETHYL PROPANOL, ACRYLATES/C10-30 ALKYL ACRYLATE
CROSSPOLYMER

WIPE OUT Antibacterial Wipes Travel Pack Lemon Scent

WIPE OUT Antibacterial Wipes Travel Pack Lemon Scent

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Decreases bacteria and germs on the skin that could cause disease

Warnings

For external use only

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin

Stop Use

Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours

Keep out of reach of children

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

Directions

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other Information

Keep containers tightly closed in a dry, cool and well ventilated place
Recommended storage temperature: 32F to 104F (0C to 40C)

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Fragrance, Water, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Tocopheryl Acetate

Hand sanitizer label

Wipe label 1

Wipe label 2

Kit label 1

Kit label 2

INGREDIENTS AND APPEARANCE

WIPE OUT SAFE PACK 
alcohol, benzalkonium chloride kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77878-014

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77878-014-01	1 in 1 KIT	08/13/2020

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	50 mL
Part 2	1 PACKET	10

Part 1 of 2

WIPE OUT HAND SANITIZER WITH MOISTURIZERS 
alcohol solution

Product Information
Item Code (Source)	NDC: 77878-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77878-012-01	50 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/13/2020

Part 2 of 2

WIPE OUT ANTIBACTERIAL WIPES TRAVEL PACK LEMON SCENT 
alcohol solution

Product Information
Item Code (Source)	NDC: 77878-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	6.8 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77878-013-01	10 in 1 PACKET; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/13/2020

Labeler - TZUMI INNOVATIONS LLC (117426322)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Meiya Display Co., Ltd.		403769687	manufacture(77878-014)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co., ltd.		421222423	manufacture(77878-012)

Establishment
Name	Address	ID/FEI	Business Operations
FuYang YangYang Health Technology Co. Ltd		529735460	manufacture(77878-013)