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

UNSCENTED HAND SANITIZER (ALCOHOL) LIQUID [UNIQUE HOLDING GROUP INC]
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NDC 25225-012-01, 25225-012-02, 25225-012-03, 25225-012-04, 25225-012-05
Set ID a058badf-6226-4fc7-86ec-43b1ce604c28
Category HUMAN OTC DRUG LABEL
Packager Unique Holding Group Inc
Generic Name
Product Class
Product Number
Application Number PART333
  • ACTIVE INGREDIENT

    Active Ingredient                                 Purpose

    Ethyl Alcohol 62%                               Sanitizer

  • DESCRIPTION

    Uses:

    To decrease bacteria on the skin that could cause diseases

    Recommended for repeated use

  • WARNINGS

    Warnings:

    For external use only-hands. Use only as directed.  Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness, or itching occurs.

    Flammable. Keep away from heat and flame.

  • WHEN USING

        When using this product

    • Keep out of eyes. In case of contacting with eyes, immediately flash with water and call a doctor.
    • Avoid contacting with a broken skin.
  • STOP USE

    Stop using and ask a doctor if irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


  • INDICATIONS & USAGE

    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 supervise while using this product.
    • May discolor certain fabrics.
  • INACTIVE INGREDIENT

    Inactive Ingredients

    aloe barbadensis gel, carbomer, deionized water, glycerin, propylene glycol, triethanolamine, and vitamin E

  • PRINCIPAL DISPLAY PANEL

    labelunscented picture

  • INGREDIENTS AND APPEARANCE
    UNSCENTED HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25225-012(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) 35.8 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
    Vitamin E (UNII: H4N855PNZ1) 0.01 g  in 100 g
    TROLAMINE (UNII: 9O3K93S3TK) 0.35 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:25225-012-0130 g in 1 BOTTLE, PLASTIC
    2NDC:25225-012-0260 g in 1 BOTTLE, PLASTIC
    3NDC:25225-012-04237 g in 1 BOTTLE, PLASTIC
    4NDC:25225-012-05500 g in 1 BOTTLE, PLASTIC
    5NDC:25225-012-03222 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33302/03/2010
    Labeler - Unique Holding Group Inc (529047265)
    Registrant - Unique Holding Group Inc (529047265)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unique Holding Group Inc529047265manufacture

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