Label: BHI SINUS- euphorbia resinifera resin, goldenseal, potassium dichromate, potassium iodide, phosphorus, pulsatilla vulgaris, and thuja occidentalis leafy twig tablet

  • 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 19, 2017

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENTS

    Each tablet contains: *Euphorbium officinarum 6X, *Hydrastis canadensis 6X, Kali bichromicum 6X, Kali iodatum 8X, *Phosphorus 8X, *Pulsatilla 4X, *Thuja occidentalis 6X 42.9 mg each.

    *Natural Ingredients

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  • INACTIVE INGREDIENTS

    Lactose and Magnesium stearate

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  • PURPOSE

    Sinus Relief Tablets

    Relieves:

    • Nasal Congestion

    • Sinus Headache & Pressure

    • Cold/Flu Nasal Symptoms

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  • USES

    For the temporary relief of minor sinus congestion and pressure due to allergic rhinitis and colds

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  • 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. Do not exceed 12 tablets in 24 hours.

    Standard dosage: Adults and children 4 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours. For children under 4, consult your health professional.

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

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  • WARNINGS

    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 Sinus or any of its ingredients exists.

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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  • BHI Sinus Tablet
  • INGREDIENTS AND APPEARANCE
    BHI SINUS 
    euphorbia resinifera resin, goldenseal, potassium dichromate, potassium iodide, phosphorus, pulsatilla vulgaris, and thuja occidentalis leafy twig tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1017
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K) EUPHORBIA RESINIFERA RESIN 6 [hp_X]
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 6 [hp_X]
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_X]
    POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION 8 [hp_X]
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 8 [hp_X]
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 4 [hp_X]
    THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 9mm
    Flavor Imprint Code Leafman
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62795-1017-2 100 in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2015
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/01/2015
    Labeler - MediNatura Inc (079324099)
    Establishment
    Name Address ID/FEI Business Operations
    MediNatura Inc 102783016 manufacture(62795-1017)
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