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 28, 2023

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

View All Sections
  • ADR-Bal

    Alteris 7X

    Eupion 15X, 30X

    Foe vul 15X

    Salix nig 15X

    Wyethia 20X

  • ADR-Bal

    Alcohol, Purified Water

  • ADR-Bal

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

  • ADR-Bal

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

  • ADR-Bal

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

  • 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.

  • ADR-Bal

    Gland Re-Balance

  • ADR-Bal

    Label

  • INGREDIENTS AND APPEARANCE
    ADR-BAL 
    adrenal support liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64616-079
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WOOD TAR HYDROCARBON DISTILLATE (UNII: 40W0G99GIW) (WOOD TAR HYDROCARBON DISTILLATE - UNII:40W0G99GIW) WOOD TAR HYDROCARBON DISTILLATE15 [hp_X]  in 1 mL
    ALETRIS FARINOSA ROOT (UNII: O021JGR97X) (ALETRIS FARINOSA ROOT - UNII:O021JGR97X) ALETRIS FARINOSA ROOT7 [hp_X]  in 1 mL
    FENNEL SEED (UNII: G3QC02NIE6) (FENNEL SEED - UNII:G3QC02NIE6) FENNEL SEED15 [hp_X]  in 1 mL
    SALIX NIGRA BARK (UNII: QU52J3A5B3) (SALIX NIGRA BARK - UNII:QU52J3A5B3) SALIX NIGRA BARK15 [hp_X]  in 1 mL
    WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (WYETHIA HELENIOIDES ROOT - UNII:J10PD1AQ0N) WYETHIA HELENIOIDES ROOT20 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64616-079-0259 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/08/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/08/2013
    Labeler - Vitality Works, Inc. (137752817)
    Registrant - Vitality Works, Inc. (137752817)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vitality Works, Inc.137752817manufacture(64616-079)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!