DYNAREX GREEN (ALCOHOL) LIQUID [DYNAREX CORPORATION]

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DYNAREX GREEN (ALCOHOL) LIQUID [DYNAREX CORPORATION]
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NDC 67777-307-01, 67777-307-02
Set ID 44f4034a-0e13-49ae-98e6-1fb627a0e930
Category HUMAN OTC DRUG LABEL
Packager Dynarex Corporation
Generic Name
Product Class
Product Number
Application Number PART333A
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  • ACTIVE INGREDIENT

    Active Ingredient                         Purpose

    Alcohol, 30% v/v                          Antiseptic

  • WARNINGS

    • For external use only
    • Flammable, keep away from fire or flame
    • Avoid contact with eyes and mucousal membranes
  • DO NOT USE

    Do not use with electrocautery procedures

  • PURPOSE

    An antiseptic wash.

  • INDICATIONS & USAGE

    Cleaning and antiseptic cleansing of skin.

  • DOSAGE & ADMINISTRATION

    Mix with water, lather and rinse off.

  • 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.

  • OTHER INFORMATION

    • Store at room temperature: 15o - 30o C (59o - 86o F)
    • Avoid excessive heat
  • INACTIVE INGREDIENTS

    Inactive ingredients: Glycerin, lavender oil, oleic acid, phenoxyethanol, potassium hydroxide, rosin, water.

  • PRINCIPAL DISPLAY PANEL

    Dynarex Green Soap

    green soap.jpg

    green soap

  • INGREDIENTS AND APPEARANCE
    DYNAREX GREEN 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-307
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.3 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    ROSIN (UNII: 88S87KL877)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-307-01473 mL in 1 BOTTLE
    2NDC:67777-307-023785 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/28/2014
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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