Label: T-42- butterfly pea 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

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

  • SPL UNCLASSIFIED SECTION

    NDC 58264-0287-1

  • INDICATIONS

    Temporary relief of symptoms associated with feeling disconnected emotionally and mentally from others and from community.

  • ACTIVE INGREDIENT

    ACTIVE

    Butterfly Pea 6X, 8X, 30X

  • INACTIVE INGREDIENT

    INACTIVE

    20% alcohol and purified water.

  • DOSAGE & ADMINISTRATION

    One dropper under tongue two times daily. Acute symptoms 1/2 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.

  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

  • PRINCIPAL DISPLAY PANEL

    DYNAMIC

    NUTRITIONAL

    ASSOCIATES

    T-42

    BUTTERFLY PEA

    FLOWER ESSENCES

    1 FL. OZ.

    T-42 DIST Label Proof 4.22.jpg

  • INGREDIENTS AND APPEARANCE
    T-42 
    butterfly pea solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0287
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLITORIA TERNATEA FLOWER (UNII: 1SYA8HK01B) (CLITORIA TERNATEA FLOWER - UNII:1SYA8HK01B) CLITORIA TERNATEA FLOWER30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0287-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/16/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/16/2022
    Labeler - DNA Labs, Inc. (031784339)