Label: NUPHARMISTO PSORIASIS ECZEMA CREAM cream

  • NDC Code(s): 83771-002-01
  • Packager: Inner Mongolia Green source pharmaceutical Products Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 7, 2024

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  • Active Ingredient

    Salicylic acid 0.2%

  • Purpose

    Antifungal

  • Use

    Temporarily protects and helps relieve minor skinirritation and itching due to: Psoriasis, Eczema, SeborrheicDermatitis,Moluscum, Shingles, Severe Boils, FungalInfections,Warts, Other Resistant Skin Conditions

  • Warnings

    For external use only

  • Do not use

    ask a doctor if Condition worsens ordoes not improve after regular use as directed

  • When Using

    When using this product "Avoid contact with eyes." lf contact occurs, rinse the eyes thoroughly with water

  • Stop Use

    Stop use & ask a doctor if Condition worsens ordoes not improve after regular use as directed

  • Ask Doctor

    Keep out of reach of childern lf swallowed, getmedical help or contact a Poison ControlCenter(1-800-222-1222)right away.

  • Keep Oot Of Reach Of Children

    Please keep the product out of reach of children. If swallowed accidentally, please call the emergency center.

  • Directions

    Apply a small amount to theproblem areas with circular motions for 3 minutes tilthe skin absorbs the cream."Apply it 2-3 times a dayfor the best result. Continue to use it for 3-5 daysafter symptoms resolve to prevent a recurrence.Do not use it on pregnant women and childrenunder 12 years of age unless directed by a doctor

  • Other information

  • Inactive ingredients

    Water, RhinacanthusNasutus, Dictamnus Dasycarpus Turcz, ViolaPhilippica, Euphorbia Hirta, Murraya Exotica,Sophora Flavescens Alt, Mentha Haplocalyx Brig.Borneolum Syntheticum, Kochia Scoparia, SmilaxGlabra Roxb, Solidago Decurrens, ChlorhexidineAcetate.

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    NUPHARMISTO PSORIASIS ECZEMA CREAM 
    nupharmisto psoriasis eczema cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83771-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    WATER (UNII: 059QF0KO0R)  
    BASSIA SCOPARIA WHOLE (UNII: 240G38P85Z)  
    RHINACANTHUS NASUTUS WHOLE (UNII: QW70YFP724)  
    EUPHORBIA HIRTA (UNII: L13YF113GN)  
    MURRAYA PANICULATA FRUIT (UNII: PE014Z7R7C)  
    SOLIDAGO DECURRENS WHOLE (UNII: Y026RJV99T)  
    VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54)  
    MENTHA CANADENSIS FLOWERING TOP (UNII: 2492Y6JJNA)  
    BORNEOL (UNII: M89NIB437X)  
    SMILAX GLABRA WHOLE (UNII: H51N91QNEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83771-002-01100 mL in 1 CANISTER; Type 0: Not a Combination Product04/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/06/2024
    Labeler - Inner Mongolia Green source pharmaceutical Products Co., LTD (699508923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inner Mongolia Green source pharmaceutical Products Co., LTD699508923label(83771-002) , manufacture(83771-002)