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

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

  • PURPOSE

    Homeopathic Combination Medicine Indications: For person surrounded by electrosmog

  • 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

  • TAMPER-EVIDENT

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

  • Direction

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

  • 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!

  • 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
  • INGREDIENTS AND APPEARANCE
    GEOVITA 
    iron, silicon dioxide, copper, formic acid, and sus scrofa cerebellum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66343-002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON6 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 1 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER21 [hp_X]  in 1 mL
    FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1) FORMIC ACID21 [hp_X]  in 1 mL
    SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (SUS SCROFA CEREBELLUM - UNII:49NGK53TPQ) SUS SCROFA CEREBELLUM21 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 0.47 mL  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66343-002-5050 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved homeopathic05/07/2015
    Labeler - RUBIMED AG (480582035)
    Establishment
    NameAddressID/FEIBusiness Operations
    RUBIMED AG480582035MANUFACTURE(66343-002)
    Establishment
    NameAddressID/FEIBusiness Operations
    Omida AG483268348MANUFACTURE(66343-002)