Label: ARSENICUM SULPHURATUM FLAVUM- arsenic trisulfide liquid

  • NDC Code(s): 71919-087-07, 71919-087-08, 71919-087-09, 71919-087-10
  • Packager: Washington Homeopathic Products
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 30, 2018

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  • ACTIVE INGREDIENTS

    ARSENICUM SULPHURATUM FLAVUM

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  • USES

    To relieve the symptoms of itchy skin.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

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  • INDICATIONS

    Indications: 

    ARSENICUM SULPHURATUM FLAVUM   Itchy skin

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  • STOP USE AND ASK DOCTOR

    If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

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  • DIRECTIONS

    Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

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  • INACTIVE INGREDIENTS

    Sucrose/Lactose

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  • PRINCIPAL DISPLAY PANEL

    The OTC potency range of ARSENICUM SULPHURATUM FLAVUM is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM.
    Label
    Availability is subject to change.

    All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

    ‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

    Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

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  • INGREDIENTS AND APPEARANCE
    ARSENICUM SULPHURATUM FLAVUM 
    arsenic trisulfide liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-087
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARSENIC TRISULFIDE (UNII: 44SIJ800OX) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRISULFIDE 30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color white (white) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:71919-087-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/14/2010
    2 NDC:71919-087-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/14/2010
    3 NDC:71919-087-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/14/2010
    4 NDC:71919-087-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/14/2010
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 12/14/2010
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    Name Address ID/FEI Business Operations
    Washington Homeopathic Products 084929389 manufacture(71919-087)
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