HAND SANITIZER 1.85OZ- alcohol gel

HAND SANITIZER 1.85OZ by

Drug Labeling and Warnings

HAND SANITIZER 1.85OZ 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 the skin.

Warnings

For external use only.

WARNINGS

Flammable. Keep away from heat and flame.

When using this product

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

irritation or redness develops.

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and rub into skin until dry.
• Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Aminomethyl Propanol, (FD&C Red No. 40, FD&C Yellow No. 5, D&C Red No. 33, FD&C Blue No.1)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 1.85OZ 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-131
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
FD&C RED NO. 40 (UNII: WZB9127XOA)
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-131-01	54.7 mL in 1 BOTTLE, PLASTIC; 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)