Label: GEOVITA- iron, silicon dioxide, copper, formic acid, and sus scrofa cerebellum liquid

  • 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 1, 2015

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  • PURPOSE

    Homeopathic Combination Medicine Indications: For person surrounded by electrosmog

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  • ACTIVE INGREDIENT

    Ingredients

    Ferrurn met. 6 x
    Silicea 12 x
    Cuprum met. 21 x
    Formicum acidum 21 x
    Cerebrum suis 21 x
    Alcohol 47 % v/v

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  • TAMPER-EVIDENT

    DO not use this product if seal at base of cap is missing or broken.

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  • Direction

    10 drops per day or as instructed by your health care provider.

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  • Warnings

    As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using the product.

    Keep out of Reach of Children!

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  • PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

    Geovita

    Homeopathic Combination
    Medicine Indications:
    For person surrounded by
    electrosmog

    RUBIMED®

    1.7 Fl.oz. (50 ml)

    Principal Display Panel - 50 ml Bottle Label
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  • INGREDIENTS AND APPEARANCE
    GEOVITA 
    iron, silicon dioxide, copper, formic acid, and sus scrofa cerebellum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-002
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 6 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 12 [hp_X]  in 1 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 21 [hp_X]  in 1 mL
    FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1) FORMIC ACID 21 [hp_X]  in 1 mL
    SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (SUS SCROFA CEREBELLUM - UNII:49NGK53TPQ) SUS SCROFA CEREBELLUM 21 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M) 0.47 mL  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66343-002-50 50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved homeopathic 05/07/2015
    Labeler - RUBIMED AG (480582035)
    Establishment
    Name Address ID/FEI Business Operations
    RUBIMED AG 480582035 MANUFACTURE(66343-002)
    Establishment
    Name Address ID/FEI Business Operations
    Omida AG 483268348 MANUFACTURE(66343-002)
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