ULTA ANTI-BACTERIAL HAND SANITIZER- alcohol gel

Ulta Anti-Bacterial Hand Sanitizer by

Drug Labeling and Warnings

Ulta Anti-Bacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ulta. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Alcohol 68%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use Decreases bacteria on hands

WARNINGS

Warnings

For external use only

WHEN USING

When using this product avoid contact with eyes

STOP USE

Stop use and ask a doctor if irritation or redness rash develops.

OTHER SAFETY INFORMATION

Flammable: Keep away from flame or high heat.

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.

DOSAGE & ADMINISTRATION

Directions: Apply sanitizer to hands. Rub hands together until dry.

INACTIVE INGREDIENT

Inactive ingredients: Aqua (water), Parfum (Fragrance), Isopropyl Alcohol, Glycerin, Carbomer, Aloe Barbadensis Leaf Extract, Triethanolamine, Lactose, Cellulose, Hydroxypropyl Methylcellulose, Benzophenone-4, Retinyl Palmitate, Tocopheryl Acetate, Ultramarine Blue, Yellow 5, Blue 1

QUESTIONS

Questions: 1-866-983-8582

SPL UNCLASSIFIED SECTION

Cleanse and condition hands without the use of water.

• Aloe helps soothe and rejuvenate
• Vitamins A & E help nourish & protect

SPL UNCLASSIFIED SECTION

NOT TESTED ON ANIMALS

MADE IN CANADA

DISTRIBUTED BY ULTA INC.

BOLINGBROOK, IL 60440

ULTA.COM

PRINCIPAL DISPLAY PANEL

ULTAbeauty™

Eucalyptus Mint

HAND SANITIZER GEL

With Aloe, Vitamins A & E

1 fl. oz./29 mL

INGREDIENTS AND APPEARANCE

ULTA ANTI-BACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62296-0047
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
ALPHA CELLULOSE (UNII: I355QGZ19A)
HYPROMELLOSES (UNII: 3NXW29V3WO)
SULISOBENZONE (UNII: 1W6L629B4K)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ULTRAMARINE BLUE (UNII: I39WR998BI)

Product Characteristics
Color	green (Light green)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62296-0047-1	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/11/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/11/2018

Labeler - Ulta (608168597)