Label: MOLLUSCUM CONTAGIOSUM TREATMENT- molluscum contagiosum treatment pen liquid

  • NDC Code(s): 82372-006-01
  • Packager: Good Manager Holdings Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated July 26, 2023

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

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

  • DO NOT USE

    DO NOT USE

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    PURPOSE

  • STOP USE

    STOP USE

  • DOSAGE & ADMINISTRATION

    DOSAGE

  • WARNINGS

    WARNING

  • WHEN USING

    WHEN USING

  • OTHER SAFETY INFORMATION

    OTHER INFORMATION

  • ASK DOCTOR

    ASK DOCTOR

  • INDICATIONS & USAGE

    USAGE

  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL

  • INGREDIENTS AND APPEARANCE
    MOLLUSCUM CONTAGIOSUM TREATMENT 
    molluscum contagiosum treatment pen liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82372-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEMONA JAPONICA ROOT (UNII: FXG254HF10)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    PHELLODENDRON CHINENSIS BARK (UNII: 2866QMZ434)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82372-006-0110 mL in 1 APPLICATOR; Type 0: Not a Combination Product07/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/26/2023
    Labeler - Good Manager Holdings Inc (118382673)
    Establishment
    NameAddressID/FEIBusiness Operations
    Good Manager Holdings Inc118382673manufacture(82372-006)