Label: BHI SKIN- berberis vulgaris root bark, graphite, hydrofluoric acid, lycopodium clavatum spore, petrolatum, toxicodendron pubescens leaf, sepia officinalis juice, and sulfur tablet

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

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 July 7, 2022

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  • ACTIVE INGREDIENTS

    Each tablet contains: *Berberis vulgaris 6X, Graphites 10X, Hydrofluoricum acidum 10X, *Lycopodium clavatum 12X, *Petroleum 10X, *Rhus toxicodendron 8X, *Sepia 10X, *Sulphur 12X 37.5 mg each.

    *Natural Ingredients

  • INACTIVE INGREDIENTS

    Inactive Ingredients: Dextrose,  Magnesium Stearate, Maltodextrin

  • PURPOSE

    Eczema Relief Tablets

    Relieves:

    • Rough Scaly Skin

    • Itching Skin

    • Redness

  • USES

    For the temporary relief of minor eczema symptoms: rough scaly skin, itching skin, redness

  • Directions

    At first sign of symptoms:Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. 

    Standard dosage: Adults and children 4 years and older: Take 1-2 tablet every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.For children under 4, consult your health professional.

    Allow tablets to dissolve completely in the mouth, do not swallow.

  • WARNINGS SECTION

    If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to BHI Skin or any of its ingredients exists.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    BHI Skin Tablet

    Add image transcription here...

  • INGREDIENTS AND APPEARANCE
    BHI SKIN 
    berberis vulgaris root bark, graphite, hydrofluoric acid, lycopodium clavatum spore, petrolatum, toxicodendron pubescens leaf, sepia officinalis juice, and sulfur tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-1016
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK6 [hp_X]
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE10 [hp_X]
    HYDROFLUORIC ACID (UNII: RGL5YE86CZ) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION10 [hp_X]
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_X]
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM10 [hp_X]
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF8 [hp_X]
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE10 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR12 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code Leafman
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-1016-31 in 1 CARTON01/01/2015
    1100 in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/2015
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    MediNatura Inc102783016manufacture(62795-1016)
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