Label: GNP GENTIAN VIOLET 1%- gentian violet 1% liquid

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

Drug Label Information

Updated December 14, 2023

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug facts

  • Active Ingredient

    Gentian Violet 1%

  • Purpose

    First Aid Antiseptic

  • Uses

    First aid to help protect against infection in minor cuts, scrapes, and burns.

  • Warnings

    For external use only.

    Do not apply to an ulcerative lesion as this may cause tatooing of the skin. Do not use in the eyes or over large areas of the body.

  • Ask a doctor before use if you have

    deep or puncture wounds, serious burns, animal bites.

  • Keep out of reach of children.

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

  • Directions

    Clean the affected area and apply directly to the wound or use cotton applicator once or twice daily. Do not bandage.

  • Other information

    will stain skin or clothing.

  • Inactive ingredients

    Ethyl Alcohol 10% and Purified Water.

  • Label

    GNP GVGNP GV 1

  • INGREDIENTS AND APPEARANCE
    GNP GENTIAN VIOLET 1% 
    gentian violet 1% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-003
    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
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24385-003-4659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/02/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2008
    Labeler - Amerrisource Bergen (007914906)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(24385-003) , analysis(24385-003) , pack(24385-003) , label(24385-003)
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!