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Zyvestra (Apotheca Company)

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TABLET 60 TABLET in 1 BOTTLE (57520-0398-1) Label Information

Complete Zyvestra Information

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Cocculus indicus 21X, 34X, 55X, Ferrum metallicum 21X, 34X, 55X, Gelsemium sempervirens 21X, 34X, 55X, Phytolacca decandra 32X, 34X, 55X, Pulsatilla 21X, 34X, 55X, Silicea 21X, 34X, 55X.



  • PURPOSE

    USES:  For the temporary relief of dizziness and nausea associated with vertigo and motion sickness.



  • WARNINGS

    WARNINGS:  Consult a physician before use:

    If pregnant or breastfeeding

    if taking other medications

    in children.

    Stop use and ask a doctor if:

    symptoms worse, persist for more that 48 hours, or reoccur

    fever develops.

    Do not use if neckband is missing or broken.

    Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.



  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  Adults:  Take one tablet daily.



  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Lactose, Magnesium stearate, Microcrystalline cellulose.


  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.



  • INDICATIONS & USAGE

    USES:  For the temporary relief of dizziness and nausea associated with vertigo and motion sickness.


  • QUESTIONS

    Questions, Comments?

    Call 1-800-741-9127

    Mfd in the USA for:   PREVAL HEALTH

    51 US Route One, Scarborough, ME 04074



  • PRINCIPAL DISPLAY PANEL

    NDC# 57520-0398-1

    ZYVESTRA

    RELIEF from symptoms associated with

    VERTIGO

    DIZZINESS

    NAUSEA

    Homeopathic Medicine

    60 Tablets

    Zyvestra


  • INGREDIENTS AND APPEARANCE
    ZYVESTRA 
    cocculus indicus, ferrum metallicum, gelsemium sempervirens, phytolacca decandra, pulsatilla, silicea, tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0398
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 55 [hp_X]
    IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 55 [hp_X]
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 55 [hp_X]
    PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 55 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 55 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (round convex) Size 6mm
    Flavor Imprint Code diamond
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57520-0398-1 60 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 12/03/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture