Label: T-22- quercus robur whole solution

  • 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 May 16, 2022

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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0267-1

  • INDICATIONS

    Despondency, despair, but never ceasing effort.

  • INGREDIENTS

    ACTIVE

    Quercus robur 6/8/30x

    INACTIVE

    20% alcohol in purified water.

  • SUGGESTED DOSAGE

    One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

  • STORAGE AND HANDLING

    SHAKE WELL

  • Warnings

    • Use only if cap seal is unbroken.

    • If pregnant or breastfeeding, ask a healthcare professional before use.

    • Keep this and all medication out of the reach of children.

    To be used according to standard homeopathic indications.

  • PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

    DYNAMIC

    NUTRITIONAL

    ASSOCIATES, INC.

    T-22

    OAK

    FLOWER ESSENCES

    1 FL. OZ.

    T-22 DIST Label Proof 4.22.jpg

  • INGREDIENTS AND APPEARANCE
    T-22 
    quercus robur whole solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0267
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W) QUERCUS ROBUR WHOLE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0267-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/1990
    Labeler - DNA Labs, Inc. (031784339)
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