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Dentastat (Energique, Inc.)

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LIQUID 30 mL in 1 PACKAGE (44911-0031-1) Label Information

Complete Dentastat Information

  • ACTIVE INGREDIENTS:

    Allium sativum 3X, Berberis vulgaris 3X, Fucus vesiculosus 3X, Phytolacca decandra 3X, Argentum metallicum 12X, Aurum metallicum 12X, Calcarea fluorica 12X, Calcarea phosphorica 12X, Iodium 12X, Mercurius solubilis 12X, Niccolum metallicum 12X, Platinum metallicum 12X, Silicea 12X, Zincum metallicum 12X.


  • INDICATIONS:

    For temporary relief of pain and minor inflammation in the mouth, or on the gums following dental procedures. **

    **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:

    For temporary relief of pain and minor inflammation in the mouth, or on the gums following dental procedures. **

    **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


  • PACKAGE LABEL DISPLAY

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    DENTASTAT

    1 fl. oz. (30 ml)

    Dentastat


  • INGREDIENTS AND APPEARANCE
    DENTASTAT 
    allium sativum, berberis vulgaris, fucus vesiculosus, phytolacca decandra, argentum metallicum, aurum metallicum, calcarea fluorica, calcarea phosphorica, iodium, mercurius solubilis, liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0031
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GARLIC (UNII: V1V998DC17) (GARLIC - UNII:V1V998DC17) GARLIC 3 [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
    FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X]  in 1 mL
    PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 3 [hp_X]  in 1 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 12 [hp_X]  in 1 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 12 [hp_X]  in 1 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 12 [hp_X]  in 1 mL
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 12 [hp_X]  in 1 mL
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 12 [hp_X]  in 1 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 12 [hp_X]  in 1 mL
    NICKEL (UNII: 7OV03QG267) (NICKEL - UNII:7OV03QG267) NICKEL 12 [hp_X]  in 1 mL
    PLATINUM (UNII: 49DFR088MY) (PLATINUM - UNII:49DFR088MY) PLATINUM 12 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 12 [hp_X]  in 1 mL
    ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 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:44911-0031-1 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/13/2012 12/22/2020
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 11/13/2012 12/22/2020
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0031)