Label: SAMSALI WART CORN REMOVER PADS- wart corn remover pads patch

  • NDC Code(s): 83818-004-01
  • Packager: Shenzhen Xinxin Yunhai Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 19, 2024

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  • Active Ingredient

    Salicylic acid 40%

  • Purpose

    Wart and Corn Remover

  • Use

    For the removal of warts and corns.

  • Warnings

    For external use only.

  • Do not use

    On irritated, infected, or reddened skin; on genital warts or warts on the face; on moles, birthmarks, or warts with hair growing from them; on mucous membranes.

  • When Using

    Avoid eye or face contact. If the product gets into eyes or faces, thoroughly rinse with water.

  • Stop Use

    Discomfort persists

  • Ask Doctor

    Diabetes; Poor blood circulation

  • Keep Oot Of Reach Of Children

    If swallowed, get medical help or contact a Poison control Center right away.

  • Directions

    wash affected area.(optional: may soak wart in warm water for 5 minutes.); dry area thoroughly. (if appropriate: cut plaster to fit wart.); apply medicated plaster; repeat procedure every 48 hours as needed until wart is removed for up to 12 weeks;

  • Other information

    store between 59° and 86°F (15°C and 30°C)

  • Inactive ingredients

    hard paraffin, lanolin, phenol, polyvinyl alkyl, vaseline

  • Questions

    Call 1-646-798-1280

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    SAMSALI WART CORN REMOVER PADS 
    wart corn remover pads patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83818-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    CLEMATIS VIORNA WHOLE (UNII: DNP609X607)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PHENOL (UNII: 339NCG44TV)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83818-004-0142 in 1 BOX; Type 0: Not a Combination Product05/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03005/14/2024
    Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xinxin Yunhai Technology Co., Ltd.699816806manufacture(83818-004)
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