Label: ADR-BAL- adrenal support 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 December 6, 2017

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  • ADR-Bal

    Alteris 7X

    Eupion 15X, 30X

    Foe vul 15X

    Salix nig 15X

    Wyethia 20X

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  • ADR-Bal

    Alcohol, Purified Water

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  • ADR-Bal

    Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

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  • ADR-Bal

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

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  • ADR-Bal

    For the temporary relief of fatigue, dizziness, general malaise, depression and exhaustion.

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  • ADR-Bal

    Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one half the adult dosage.

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  • ADR-Bal

    Gland Re-Balance

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  • ADR-Bal
  • INGREDIENTS AND APPEARANCE
    ADR-BAL 
    adrenal support liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:64616-079
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALETRIS FARINOSA ROOT (UNII: O021JGR97X) (ALETRIS FARINOSA ROOT - UNII:O021JGR97X) ALETRIS FARINOSA ROOT 7 [hp_X]  in 1 mL
    FENNEL SEED (UNII: G3QC02NIE6) (FENNEL SEED - UNII:G3QC02NIE6) FENNEL SEED 15 [hp_X]  in 1 mL
    SALIX NIGRA BARK (UNII: QU52J3A5B3) (SALIX NIGRA BARK - UNII:QU52J3A5B3) SALIX NIGRA BARK 15 [hp_X]  in 1 mL
    WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (WYETHIA HELENIOIDES ROOT - UNII:J10PD1AQ0N) WYETHIA HELENIOIDES ROOT 20 [hp_X]  in 1 mL
    WOOD TAR HYDROCARBON DISTILLATE (UNII: 40W0G99GIW) (WOOD TAR HYDROCARBON DISTILLATE - UNII:40W0G99GIW) WOOD TAR HYDROCARBON DISTILLATE 15 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64616-079-02 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 04/08/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/08/2013
    Labeler - Vitality Works, Inc. (137752817)
    Registrant - Vitality Works, Inc. (137752817)
    Establishment
    Name Address ID/FEI Business Operations
    Vitality Works, Inc. 137752817 manufacture(64616-079)
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