Label: MEOLY WART REMOVAL CREAM 20G- wart removal cream 20g ointment

  • NDC Code(s): 83818-008-01
  • Packager: Shenzhen Xinxin Yunhai Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 16, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active Ingredient

    Salicylic Acid 1.5%

  • Purpose

    Wart Removal

  • Use

    For the removal of common warts, plantar warts, flat warts, corns, and calluses.

  • Warnings

    For external use only. Please keep out of reach of children.

  • Do not use

    On the eye area. On damaged or cut skin, like wounds, grazes, eczema, sunburn, etc. If you have a known allergy to this product.

  • When Using

    Keep out of eyes, ears, mouth, and any open hurt skin area. In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop Use

    Stop using and ask a doctor if irritation or rash occurs.

  • Ask Doctor

    stop using andask a doctor if irritation orrash occurs.

  • Keep Out of Reach of Children

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

  • Directions

    1. Wash the affected area, may soak in warm water for about 5 minutes for better results.
    2. Pat dry the area and use the applicator cotton swab.
    3. Apply a layer of the ointment to sufficiently cover each wart.
    4. Allow fully absorb and cover with a bandage if needed.
    5. Repeat the procedure twice a day for around 4 weeks.

  • Other information

    Keep the cream in a dry and shaded place.

  • Inactive ingredients

    Bassia Scoparia, Crocus Sativus, Sophora Flavescens, Typhonium Giganteum Stem.

  • Questions

    Contact us at support@meolycare.com

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    MEOLY WART REMOVAL CREAM 20G 
    wart removal cream 20g ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83818-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    TYPHA ANGUSTIFOLIA STEM (UNII: OIS20S41EB)  
    BASSIA SCOPARIA WHOLE (UNII: 240G38P85Z)  
    SAFFRON (UNII: E849G4X5YJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83818-008-0120 g in 1 TUBE; Type 0: Not a Combination Product12/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02812/17/2024
    Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xinxin Yunhai Technology Co., Ltd.699816806manufacture(83818-008)