Label: REINREUDE TAG WART- salicylic acid 40% tag wart patch

  • NDC Code(s): 84010-054-01
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 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 mempranes.

  • When Using

    Avoid contact with eyes or face. lf the product gets into the eyes, rinse thoroughly with water.

  • Stop Use

    Discomfort persists

  • Ask Doctor

    Ask a doctor if you have diabetes or poor blood circulation.

  • Keep Oot Of Reach Of Children

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

  • Directions

    Wash the affected area. (Optional: soak the wart in warm water for 5 minutes.Dry the area thoroughly. lf needed, cut the plaster to fit the wart. Apply the medicated plaster. Repeat every 48 hours as needed, for up to 12 weeks.

    Other information: Store between 59°F and 86°F(15°C and 30°C).

  • Inactive ingredients

    hard paraffin,lanolin,phenol, petrolatum

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    REINREUDE TAG WART 
    salicylic acid 40% tag wart patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-054
    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
    LANOLIN (UNII: 7EV65EAW6H)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PHENOL (UNII: 339NCG44TV)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-054-0142 in 1 BOX; Type 0: Not a Combination Product12/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02812/16/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056manufacture(84010-054)
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