PREVAIL HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol gel

PREVAIL Hand Sanitizer with Moisturizers and Vitamin E by

Drug Labeling and Warnings

PREVAIL Hand Sanitizer with Moisturizers and Vitamin E by is a Otc medication manufactured, distributed, or labeled by Major Surplus And Survival Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

● For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are  not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• On children less than 2 months of age
• On open skin wounds

When using this product

do not use in or near eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly wit hwater

Stop use and ask a doctor

if irritation or rash appears on the skin

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

● Place enough product on hands to cover all surfaces. Rub handst ogether until dry. 

● Children under 6 years of age should be supervised by adult when applying this product. 

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F) 
• May discolor certain fabrics or surfaces

Inactive ingredients

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

Package Labeling: 60ml

Package Labeling: 250ml

Package Labeling: 500ml

Package Labeling: 1000ml

INGREDIENTS AND APPEARANCE

PREVAIL HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79446-028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SQUALANE (UNII: GW89575KF9)
PANTHENOL (UNII: WV9CM0O67Z)
INULIN (UNII: JOS53KRJ01)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
FRUCTOSE (UNII: 6YSS42VSEV)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79446-028-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020	01/31/2026
2	NDC: 79446-028-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020	01/31/2026
3	NDC: 79446-028-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020	01/31/2026
4	NDC: 79446-028-04	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/16/2020	01/31/2026

Labeler - Major Surplus And Survival Inc. (789081502)