D-79 (URTICA URENS, TOXICODENDRON PUBESCENS LEAF, AND ECHINACEA ANGUSTIFOLIA) SOLUTION [DNA LABS, INC.]

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D-79 (URTICA URENS, TOXICODENDRON PUBESCENS LEAF, AND ECHINACEA ANGUSTIFOLIA) SOLUTION [DNA LABS, INC.]
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NDC 58264-0080-1
Set ID 0dd8244d-4cd4-4fa8-980a-6089278824dc
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0080-1

  • INDICATIONS

    Allergy to poison oak or ivy.

  • INGREDIENTS

    ACTIVE

    Urtica urens 3x, Rhus toxicodendron 3x, Echinacea angustifolia 2x

    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.
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

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

    DYNAMIC
    NUTRITIONAL
    ASSOCIATES, INC.

    D 79

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    D-79 
    urtica urens, toxicodendron pubescens leaf, and echinacea angustifolia solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0080
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Urtica urens (UNII: IHN2NQ5OF9) (Urtica urens - UNII:IHN2NQ5OF9) Urtica urens3 [hp_X]  in 1 mL
    Toxicodendron pubescens leaf (UNII: 6IO182RP7A) (Toxicodendron pubescens leaf - UNII:6IO182RP7A) Toxicodendron pubescens leaf3 [hp_X]  in 1 mL
    Echinacea angustifolia (UNII: VB06AV5US8) (Echinacea angustifolia - UNII:VB06AV5US8) Echinacea angustifolia2 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0080-129.57 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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