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Renastat (Energique, Inc.)

Available Formats

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LIQUID 30 mL in 1 BOTTLE, DROPPER (44911-0033-1) Label Information

Complete Renastat Information

  • ACTIVE INGREDIENTS

    Berberis Vulgaris 3X, Petroselinum Sativum 3X, Sabal Serrulata 3X, Uva Ursi 3X, Cantharis 12X, Lithium Carbonicum 12X, Mercurius Corrosivus 12X, Pareira Brava 12X, Sarsparilla 12X, Solidago Virgaurea 12X.


  • INDICATIONS

    For temporary relief of pain in the abdomen extending around to the back, pain in the thighs and loins on urinating and frequent urination.

    These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.


  • WARNINGS

    If pregnant or breast-feeding, ask a health professional before use.

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

    Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.


  • DIRECTIONS

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.


  • INACTIVE INGREDIENTS

    Demineralized water, 20% Ethanol.


  • KEEP OUT OF REACH OF CHILDREN

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


  • INDICATIONS AND USAGE

    For temporary relief of pain in the abdomen extending around to the back, pain in the thighs and loins on urinating and frequent urination.

    These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.


  • QUESTIONS

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078


  • PRINCIPAL DISPLAY PANEL

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    RENASTAT

    1 fl oz (30 ml)

    Renastat


  • INGREDIENTS AND APPEARANCE
    RENASTAT 
    berberis vulgaris, petroselinum sativum, sabal serrulata, uva ursi, cantharis, lithium carbonicum, mercurius corrosivus liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0033
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SAW PALMETTO (UNII: J7WWH9M8QS) (SAW PALMETTO - UNII:J7WWH9M8QS) SAW PALMETTO 3 [hp_X]  in 1 mL
    LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA 12 [hp_X]  in 1 mL
    LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM CARBONATE 12 [hp_X]  in 1 mL
    MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 12 [hp_X]  in 1 mL
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X]  in 1 mL
    PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (PETROSELINUM CRISPUM - UNII:1WZA4Y92EX) PETROSELINUM CRISPUM 3 [hp_X]  in 1 mL
    ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (ARCTOSTAPHYLOS UVA-URSI LEAF - UNII:3M5V3D1X36) ARCTOSTAPHYLOS UVA-URSI LEAF 3 [hp_X]  in 1 mL
    CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z) (CHONDRODENDRON TOMENTOSUM ROOT - UNII:395A3P448Z) CHONDRODENDRON TOMENTOSUM ROOT 12 [hp_X]  in 1 mL
    SMILAX REGELII ROOT (UNII: 2H1576D5WG) (SARSAPARILLA - UNII:2H1576D5WG) SMILAX REGELII ROOT 12 [hp_X]  in 1 mL
    SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44911-0033-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/04/2012
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0033)