Label: GENTIAN VIOLET ANTI-INFECTIVE- gentian violet 1% liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 27, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient

    Gentian Violet 1%

  • Purpose

    First Aid Antiseptic

  • Uses

    As first aid to help prevent skin infection in minor cuts n scrapes n burns
    Warnings n For external use only

  • Warnings

    For external use only
    Ask a doctor before use. if you have deep or puncture wounds, animal bites or serious burns. When using this product. do not use in eyes or apply over large areas of the body. do not use longer than 1 week unless directed by a doctor.
    Stop use and ask a doctor if condition persists or gets worse

  • Ask a Doctor before use if

    You have deep or puncture wounds, animal bites or serious burns.

  • Keep out of reach of children.

    Keep out of the reach of children. If swallowed, get medical
    help or contact a Poison Control Center right away.

  • Directions

    Clean the affected area, apply a small amount on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

  • Other Information

    Product will stain skin and clothing.

  • Inactive Ingredients

    Ethyl alcohol 10%, and purified water.

  • Questions or Comments

    1-305-256-1464

  • Principal Display Panel

    Gentian Violet Gentian Violet

  • INGREDIENTS AND APPEARANCE
    GENTIAN VIOLET  ANTI-INFECTIVE
    gentian violet 1% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73635-1219
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GENTIAN VIOLET (UNII: J4Z741D6O5) (GENTIAN VIOLET CATION - UNII:3GVJ31T6YY) GENTIAN VIOLET10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73635-1219-129.62 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/29/2021
    Labeler - Germa Products, LLC (116626935)
    Registrant - Germa Products, LLC (116626935)
    Establishment
    NameAddressID/FEIBusiness Operations
    World Perfume, Inc.101312044manufacture(73635-1219)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!