G-7 (BETULA PUBESCENS FLOWER BUD AND BETULA PENDULA LEAF) SOLUTION [DNA LABS, INC.]

G-7 (BETULA PUBESCENS FLOWER BUD AND BETULA PENDULA LEAF) SOLUTION [DNA LABS, INC.]
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NDC 58264-0370-2
Set ID 4f45aef4-def2-4464-9a17-19db9cb64985
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0370-2

  • INDICATIONS & USAGE

    INDICATIONS

    Painful joints, allergies, fatigue.

  • INGREDIENTS

    ACTIVE

    Betula (Birch) 1DH

    INACTIVE

    36.6% alcohol (V/V) Glycerin Macerate

  • Rx CAUTION

    Federal law prohibits dispensing without a prescription.

  • SUGGESTED DOSAGE

    One dropper full twice daily.

  • 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 - 2 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL
    ASSOCIATES, INC.

    G-7

    BETULA

    GEMMOTHERAPY

    2 FL. OZ.

    Principal Display Panel - 2 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    G-7 
    betula pubescens flower bud and betula pendula leaf solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0370
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA PUBESCENS FLOWER BUD (UNII: 32JS91VU1G) (BETULA PUBESCENS FLOWER BUD - UNII:32JS91VU1G) BETULA PUBESCENS FLOWER BUD1 [hp_X]  in 1 mL
    BETULA PENDULA LEAF (UNII: 5HW39H9KDH) (BETULA PENDULA LEAF - UNII:5HW39H9KDH) BETULA PENDULA LEAF1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0370-259.14 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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