VANILLA FIG HAND SANITIZER (ALCOHOL) LIQUID [UNIQUE HOLDING GROUP INC]

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VANILLA FIG HAND SANITIZER (ALCOHOL) LIQUID [UNIQUE HOLDING GROUP INC]
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NDC 25225-018-01, 25225-018-02, 25225-018-03, 25225-018-04, 25225-018-05
Set ID 5b0687de-537c-45b9-b264-800ec942d009
Category HUMAN OTC DRUG LABEL
Packager Unique Holding Group Inc
Generic Name
Product Class
Product Number
Application Number PART333E
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  • ACTIVE INGREDIENT

    Active Ingredient

    Ethyl Alcohol 62%  

  • PURPOSE


    Purpose:

    Sanitizer
  • INDICATIONS & USAGE


    Uses:

    To decrease the bacteria on the skin that could cause disease. Recommended for repeated use.
  • WARNINGS


    Warnings:

    For external use only-hands.
    Use only as directed.
    Excessive use or prolonged exposure may cause irritation to the skin.
    Discontinue use if irritation, redness, or itching occurs.
    Flammable. Keep away from heat and flame
  • WHEN USING

    When Using This Product:

    Keep out of eyes. In case of contact with eyes, flush immediately with water and call a doctor.

    Avoid contact with broken skin


  • ASK DOCTOR


    Stop Use And Ask A Doctor if irritation or redness develops


  • KEEP OUT OF REACH OF CHILDREN



    Keep Out of Reach of Children

    In case ofaccidental ingestion, seek professional assistance or contact a Poison Control Center immediately
  • DOSAGE & ADMINISTRATION

    Directions:

    Put a thumb size amount in your palm and rub hands together briskly until dry

  • STORAGE AND HANDLING

    Other Information

    Do not store in temperatures over 118F

    Children under six years of age should be supervised while using this product.

    May discolor certain fabrics

  • INACTIVE INGREDIENT



    Inactive Ingredients

    aloe barbadensis gel, carbomer, deionized water, Fragrance, glycerin, propylene glycol, D and C Red No. 33, triethanolamine, and vitamin E

  • PRINCIPAL DISPLAY PANEL

    labelabel

  • INGREDIENTS AND APPEARANCE
    VANILLA FIG HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25225-018(NDC:None)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R) 35.5998 g  in 100 g
    Propylene Glycol (UNII: 6DC9Q167V3) 0.5 g  in 100 g
    Glycerin (UNII: PDC6A3C0OX) 1 g  in 100 g
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.01 g  in 100 g
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) 0.33 g  in 100 g
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) 0.01 g  in 100 g
    TROLAMINE (UNII: 9O3K93S3TK) 0.35 g  in 100 g
    VANILLA (UNII: Q74T35078H) 0.2 g  in 100 g
    D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.0002 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:25225-018-0128 g in 1 BOTTLE, PLASTIC
    2NDC:25225-018-0259 g in 1 BOTTLE, PLASTIC
    3NDC:25225-018-04237 g in 1 BOTTLE, PLASTIC
    4NDC:25225-018-05500 g in 1 BOTTLE, PLASTIC
    5NDC:25225-018-03222 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/13/2010
    Labeler - Unique Holding Group Inc (529047265)
    Registrant - Unique Holding Group Inc (529047265)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unique Holding Group Inc529047265manufacture
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