Label: DYNAREX GREEN- alcohol liquid

  • NDC Code(s): 67777-308-01, 67777-308-02, 67777-308-03, 67777-308-11, view more
    67777-308-12
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2024

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

    Inactive ingredients: Coconut acid, fragrance, glycerin, oleic acid, potassium hydroxide, water.

  • Label

    1363 IN GVIN010

  • Label

    1362 IN GVIN010

  • INGREDIENTS AND APPEARANCE
    DYNAREX GREEN 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-308
    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
    OLEIC ACID (UNII: 2UMI9U37CP)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-308-1112 in 1 CASE07/01/2014
    1NDC:67777-308-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:67777-308-124 in 1 CASE07/01/2014
    2NDC:67777-308-023785 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:67777-308-0359 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/2014
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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