UBERLISS HAND SANITIZER- ethyl alcohol gel

Uberliss by

Drug Labeling and Warnings

Uberliss by is a Otc medication manufactured, distributed, or labeled by Salon Commodities, Inc., Avlon Industries Inc. 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 when hand washing is not an option.

Warnings

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

STOP USE

Stop use and ask a doctor if irritation or rash appears and lasts

WHEN USING

When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Put enough product in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using Überliss® Hand Sanitizer

Other Information

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

Inactive Ingredients

Water/Aqua/Eau, Betaine, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Carbomer, Aminomethyl Propanol

Package Label - Principal Display Panel

3.7 fl oz/110 mL

NDC: 72474-105-01

INGREDIENTS AND APPEARANCE

UBERLISS  HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72474-105
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
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
BETAINE (UNII: 3SCV180C9W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72474-105-01	110 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/06/2020

Labeler - Salon Commodities, Inc. (046900541)

Registrant - Avlon Industries Inc (121278626)

Establishment
Name	Address	ID/FEI	Business Operations
Avlon Industries Inc		121278626	manufacture(72474-105)