Ulta Beauty Hand Sanitizer Kit

Ulta Beauty Hand Sanitizer by

Drug Labeling and Warnings

Ulta Beauty Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by BASE4 Ventures, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ULTA BEAUTY HAND SANITIZER- alcohol 
BASE4 Ventures, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Ulta Beauty Hand Sanitizer Kit

Drug Facts

Active Ingredient

Alcohol 66%

Purpose

Antiseptic

Use

Decreases bacteria on hands

Warnings

For external use only Flammable: Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor 

if irritation or rash develops.

Keep out of reach of children.

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

Directions

Apply sanitizer to hands. Rub hands together until dry.

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, Water.

Questions

1-866-983-8582

Package Labeling:62651-028-01

Package Labeling:62651-029-01

Package Labeling:62651-030-01

Package Labeling:62651-031-01

ULTA BEAUTY HAND SANITIZER 
alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-038

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-038-00	1 in 1 KIT	10/15/2020	10/01/2021

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	29 mL
Part 2	1 BOTTLE	29 mL
Part 3	1 BOTTLE	29 mL
Part 4	1 BOTTLE	29 mL

Part 1 of 4

HAND SANITIZER WHIPPED VANILLA 
alcohol gel

Product Information
Item Code (Source)	NDC: 62651-028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.66 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-028-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020

Part 2 of 4

HAND SANITIZER BERRY TART 
alcohol gel

Product Information
Item Code (Source)	NDC: 62651-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.66 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-029-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020

Part 3 of 4

HAND SANITIZER MERRY BERRY 
alcohol gel

Product Information
Item Code (Source)	NDC: 62651-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.66 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-030-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020

Part 4 of 4

HAND SANITIZER SUGAR COOKIE 
alcohol gel

Product Information
Item Code (Source)	NDC: 62651-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.66 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-031-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020	10/01/2021

Labeler - BASE4 Ventures, Inc (137316126)

Revised: 9/2021

Document Id: cb934de9-dbb6-1b2d-e053-2995a90a39ce

34390-5

Set id: a9df75f2-ac7a-4e7b-e053-2995a90a239d

Version: 3

Effective Time: 20210909