Ulta Freshwater Mist Anti-Bacterial Hand Sanitizer

Dosage form: gel
Ingredients: ALCOHOL 68mL in 100mL
Labeler: Ulta
NDC Code: 62296-0042

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.

DRUG FACTS:

Active ingredient:                     Purpose 

Alcohol 68% .........................Antiseptic


USE: 

Decreases bacteria on hands.

Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center right away.

Warnings

For external use only

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When using this product keep out of eyes.

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Stop use and ask doctor if irritation or redness develops.  I

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Flammable:  Keep away from flame or high heat.

Directions - Rub a dime sized drop into hands.



Directions - Rub a dime sized drop into hands.

Inactive Ingredients

Water, Fragrance, Isopropyl Alcohol, Glycerin, Aloe Barbadenis Leaf Juice,

Carbomer, Triethanolamine, Lactose, Cellulose, Hydroxypropyl Methylcellulose,

Benzophenone-4, Retinyl Palmitate, Tocopheryl Acetate, Ultramarine Blue, Blue 1


ULTA FRESHWATER MIST ANTI-BACTERIAL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62296-0042
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL68 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water 
ISOPROPYL ALCOHOL 
GLYCERIN 
ALOE VERA LEAF 
CARBOMER HOMOPOLYMER TYPE C 
TROLAMINE  
ANHYDROUS LACTOSE 
ALPHA CELLULOSE 
HYPROMELLOSES 
SULISOBENZONE 
VITAMIN A PALMITATE 
ALPHA-TOCOPHEROL ACETATE 
Product Characteristics
Coloryellow (FD&C yellow no. 5) , blue (Ultramarine blue) Score    
ShapeSize
FlavorLEMON (Fragrance) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:62296-0042-129 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/2011
Labeler - Ulta (608168597)
Registrant - Willard Manufacturing Inc. (208799143)
Establishment
NameAddressID/FEIOperations
Willard Manufacturing Inc.208799143manufacture

Revised: 06/2011
 
Ulta

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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