Label: NUPHARMISTO PSORIASIS ECZEMA CREAM- psoriasis eczema cream cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 23, 2023

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  • Active Ingredient

    RHINACANTHUS NASUTUS 7%
    DICTAMNUS DASYCARPUS TURCZ 7%
    VIOLA PHILIPPICA 3%
    EUPHORBIA HIRTA 2%
    MURRAYA EXOTICA 2%
    SOPHORA FLAVESCENS ALT 1.8%
    MENTHA HAPLOCALYX BRIQ 1.2%

  • Purpose

    Relieve the itching, dry and scaling

  • Use

    Temporarily protects and helps relieveminor skin irritation and itching due to: PsoriasisEczema, Seborrheic Dermatitis, Molluscum,Shingles, Severe Boils, Fungal lnfections, Warts.Other Resistant Skin Conditions

  • Warnings

    For external use only.

  • WHEN USING SECTION

    Avoid contact with eyeslf contact occurs, rinse the eyes thoroughly with water

  • STOP USE section

    Condition worsens ordoes not improve after regular use as directed

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, getmedical help or contact aPoison Control Center(1-800-222-1222) right away.

  • ASK DOCTOR

    Apply a thin layer over the affected areatwice daily(morning and night), or asdirected by a doctor.
    If the condition persists longer, consult a doctor.

  • Directions

    Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.

  • Other information

    Store at 59-86ff(15-30°CClose the cap tightly after use.

  • Inactive ingredients

    Smilax Glabra, Sophora Flavescens, CnidiumMonnier(L) Cuss, Fructus Kochiae, Pseudolarixamabillis, Cortex Dictamni, Stemonatuberosalour, Mentha, Glycyrrhetinic Acid

  • PACKAGE LABEL - PRINCIPAL DISPLAY PANEL

    81799-010-01

    81799-010-01

  • INGREDIENTS AND APPEARANCE
    NUPHARMISTO PSORIASIS ECZEMA CREAM 
    psoriasis eczema cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81799-010
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHA CANADENSIS TOP (UNII: 610T51U707) (MENTHA CANADENSIS TOP - UNII:610T51U707) MENTHA CANADENSIS TOP1.2 mg  in 100 mL
    VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54) (VIOLA PHILIPPICA WHOLE - UNII:O176VC3N54) VIOLA PHILIPPICA WHOLE3 mg  in 100 mL
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) (SOPHORA FLAVESCENS WHOLE - UNII:X8KX602M5L) SOPHORA FLAVESCENS WHOLE1.8 mg  in 100 mL
    RHINACANTHUS NASUTUS LEAF (UNII: 97OQD55S9I) (RHINACANTHUS NASUTUS LEAF - UNII:97OQD55S9I) RHINACANTHUS NASUTUS LEAF7 mg  in 100 mL
    DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH) (DICTAMNUS DASYCARPUS WHOLE - UNII:IM7ZCU30YH) DICTAMNUS DASYCARPUS WHOLE7 mg  in 100 mL
    EUPHORBIA HIRTA (UNII: L13YF113GN) (EUPHORBIA HIRTA - UNII:L13YF113GN) EUPHORBIA HIRTA2 mg  in 100 mL
    MURRAYA PANICULATA FRUIT (UNII: PE014Z7R7C) (MURRAYA PANICULATA FRUIT - UNII:PE014Z7R7C) MURRAYA PANICULATA FRUIT2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORNEOL (UNII: M89NIB437X)  
    SMILAX GLABRA WHOLE (UNII: H51N91QNEB)  
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    SCOPARIA DULCIS LEAF (UNII: 1PD9Z8123P)  
    SOLIDAGO DECURRENS WHOLE (UNII: Y026RJV99T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81799-010-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM03203/15/2023
    Labeler - Ehy Holdings LLC (117322715)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ehy Holdings LLC117322715manufacture(81799-010)
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