EVERWIPE HAND SANITIZER- alcohol gel

Everwipe hand Sanitizer by

Drug Labeling and Warnings

Everwipe hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brands International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol, 70% v/v

INDICATIONS & USAGE

Antiseptic skin cleanser

Purpose

Antiseptic (skin) cleanser

Warnings

For external use only. Flammable, keep away from fire or flame.

When using this product.

• If contact occurs, rinse thoroughly with water.
• avoid contact with eyes.

Stop use and ask a doctor if irritation  develops.

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

Directions

• place enough product on your plam to thoroughly cover your hands
• rub thoroughly into hands for at least 30 seconds
• Allow to dry

Other Information

• Store below 43°C (110°F)
• may discolor certain fabrics or surfaces.

Inactive Ingredients

Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Glycerin, Propylene glycol, Water, Tocopheryl Acetate (Vit E).

Isopropyl Alcohol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EVERWIPE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-518
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-518-44	443 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/11/2021
2	NDC: 50157-518-37	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/11/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/11/2021

Labeler - Brands International (243748238)

Registrant - Brands International (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International		243748238	manufacture(50157-518)