ULTA ANTI-BACTERIAL HAND SANITIZER (ALCOHOL) GEL [ULTA]

ULTA ANTI-BACTERIAL HAND SANITIZER (ALCOHOL) GEL [ULTA]
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NDC 62296-0047-1
Set ID 6e8b257c-0652-9de0-e053-2991aa0ad901
Category HUMAN OTC DRUG LABEL
Packager Ulta
Generic Name
Product Class
Product Number
Application Number PART333E
  • 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

    ULTA eucalyptus mint HS

  • INGREDIENTS AND APPEARANCE
    ULTA ANTI-BACTERIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62296-0047
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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
    Colorgreen (Light green) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62296-0047-129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/11/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/11/2018
    Labeler - Ulta (608168597)
    Registrant - Willard Manufacturing Inc. (208799143)
    Establishment
    NameAddressID/FEIBusiness Operations
    Willard Manufacturing Inc.208799143manufacture(62296-0047)

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