U INSTANT HAND SANITIZER CLASSIC 8OZ- ethyl alcohol gel

U INSTANT HAND SANITIZER CLASSIC 8OZ by

Drug Labeling and Warnings

U INSTANT HAND SANITIZER CLASSIC 8OZ by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredient

Ethyl Alcohol 70 percent

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

Flammable. Keep away from fire or flame.

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 doctor if irritation or rash appears and lasts.

Keep out of reach for children.

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

Directions

• Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using this product.

Other Information:

• Store below 106 Fahrenheit (41 Degree Celsius)
• May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS:

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

U INSTANT HAND SANITIZER CLASSIC 8OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-205
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 934 (UNII: Z135WT9208)
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-205-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - Universal Distribution Center LLC (019180459)

Registrant - Universal Distribution Center LLC (019180459)