Label: PSORIASIS HP- arsenic trioxide, sodium borate, graphite, sodium chloride, sepia officinalis juice and sulfur liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 11/10

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Arsenicum album 30X, Borax 30X, Graphites 30X, Natrum muriaticum 30X, Sepia 30X, Sulphur 30X.

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  • PURPOSE

    INDICATIONS:  For temporary relief of symptoms due to skin eruptions and psoriasis.


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  • WARNINGS

    WARNINGS:  If pregnant or breast-feeding, ask a health care professional before use.

    Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

    Do not use if tamper evident seal is broken or missing.  Store in a cool, dry place.


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  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  10 drops orally, 3 times a day.  Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.


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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.


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  • INDICATIONS & USAGE

    INDICATIONS:  For temporary relief of symptoms due to skin eruptions and psoriasis.

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  • QUESTIONS


    Distributed by:

    BIOACTIVE NUTRITIONAL

    Melbourne, FL 32935


    For Nutritional Information write:

    BioActive Nutritional, Inc.

    1803 N. Wickham Rd.

    Melbourne, FL 32935


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  • PRINCIPAL DISPLAY PANEL

    BioActive Homeopathic

    PSORIASIS HP

    1 FL OZ (30 ml)

    Psoriasis HP

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  • INGREDIENTS AND APPEARANCE
    PSORIASIS  HP
    arsenicum album, borax, graphites, natrum muriaticum, sepia, sulphur, liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:57520-0353
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARSENIC TRIOXIDE (ARSENIC TRIOXIDE) ARSENIC TRIOXIDE 30 [hp_X]  in 1 mL
    SODIUM BORATE (SODIUM CATION) SODIUM BORATE 30 [hp_X]  in 1 mL
    GRAPHITE (GRAPHITE) GRAPHITE 30 [hp_X]  in 1 mL
    SODIUM CHLORIDE (SODIUM CATION) SODIUM CHLORIDE 30 [hp_X]  in 1 mL
    SEPIA OFFICINALIS JUICE (SEPIA OFFICINALIS JUICE) SEPIA OFFICINALIS JUICE 30 [hp_X]  in 1 mL
    SULFUR (SULFUR) SULFUR 30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57520-0353-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 11/10/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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