2PK HAND SANITIZER CLASSIC- alcohol gel

2PK HAND SANITIZER CLASSIC by

Drug Labeling and Warnings

2PK HAND SANITIZER CLASSIC by is a Otc medication manufactured, distributed, or labeled by UNIVERSAL DISTRIBUTION CENTER LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62%

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 a doctor if

irritation or rash appears and lasts.

Keep out of reach of 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℉ (41℃)
• May Discolor certain fabrics or surfaces.

Inactive ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Aminomethyl Propanol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

2PK HAND SANITIZER CLASSIC 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-132
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-132-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2018
2	NDC: 52000-132-12	120 mL in 1 BLISTER PACK; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/01/2018

Labeler - UNIVERSAL DISTRIBUTION CENTER LLC (019180459)

Registrant - UNIVERSAL DISTRIBUTION CENTER LLC (019180459)