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WIPE OUT Safe Pack

Dosage form: kit
Ingredients: ALCOHOL 75mL in 100mL; BENZALKONIUM CHLORIDE 6.8mg
Labeler: TZUMI INNOVATIONS LLC
NDC code: 77878-014

Medically reviewed by Drugs.com. Last updated on Aug 7, 2024.

Wipe Out! Safe Pack (style# 7686HD)

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

WIPE OUT SAFE PACK 
alcohol, benzalkonium chloride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77878-014
Packaging
#Item CodePackage Description
1NDC:77878-014-011 KIT in 1 KIT
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 50 mL
Part 21 PACKET 10 
Part 1 of 2
WIPE OUT HAND SANITIZER WITH MOISTURIZERS 
alcohol solution
Product Information
Item Code (Source)NDC:77878-012
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
ALOE VERA LEAF 
AMINOMETHYLPROPANOL 
Packaging
#Item CodePackage Description
1NDC:77878-012-0150 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/13/2020
Part 2 of 2
WIPE OUT ANTIBACTERIAL WIPES TRAVEL PACK LEMON SCENT 
alcohol solution
Product Information
Item Code (Source)NDC:77878-013
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE6.8 mg
Inactive Ingredients
Ingredient NameStrength
WATER 
ALOE VERA LEAF 
PROPYLENE GLYCOL 
POLYSORBATE 20 
PHENOXYETHANOL 
.ALPHA.-TOCOPHEROL ACETATE 
Packaging
#Item CodePackage Description
1NDC:77878-013-0110 SOLUTION in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/13/2020
Labeler - TZUMI INNOVATIONS LLC (117426322)
Establishment
NameAddressID/FEIOperations
Shenzhen Lantern Science Co., ltd.421222423manufacture(77878-012)
Establishment
NameAddressID/FEIOperations
FuYang YangYang Health Technology Co. Ltd529735460manufacture(77878-014, 77878-013)

Revised: 08/2020
 
TZUMI INNOVATIONS LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.