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
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 28, 2022

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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 not finalpart333A07/01/2014
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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