D-59 (FUCUS VESICULOSUS, SPONGIA OFFICINALIS SKELETON, ROASTED, GRAPHITE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, AND CROTON OIL) SOLUTION [DNA LABS, INC.]

D-59 (FUCUS VESICULOSUS, SPONGIA OFFICINALIS SKELETON, ROASTED, GRAPHITE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, AND CROTON OIL) SOLUTION [DNA LABS, INC.]
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NDC 58264-0059-1
Set ID b153cf23-eb3b-4647-b7f4-44380d498334
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0059-1

  • INDICATIONS

    Tendency to put on weight, slimming effect.

  • INGREDIENTS

    ACTIVE

    Fucus vesiculosus 3x, Spongia tosta 3x, Graphites 12x, Calcarea carbonica 12x, Natrum sulfuricum 2x, Croton tiglium 4x

    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 59

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    D-59 
    fucus vesiculosus, spongia officinalis skeleton, roasted, graphite, oyster shell calcium carbonate, crude, sodium sulfate, and croton oil solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0059
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Fucus vesiculosus (UNII: 535G2ABX9M) (Fucus vesiculosus - UNII:535G2ABX9M) Fucus vesiculosus3 [hp_X]  in 1 mL
    Spongia officinalis skeleton, roasted (UNII: 1PIP394IID) (Spongia officinalis skeleton, roasted - UNII:1PIP394IID) Spongia officinalis skeleton, roasted3 [hp_X]  in 1 mL
    Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O) Graphite12 [hp_X]  in 1 mL
    Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I) Oyster shell calcium carbonate, crude12 [hp_X]  in 1 mL
    Sodium sulfate (UNII: 0YPR65R21J) (Sodium sulfate anhydrous - UNII:36KCS0R750) Sodium sulfate2 [hp_X]  in 1 mL
    Croton oil (UNII: WK97EQG57S) (Croton oil - UNII:WK97EQG57S) Croton oil4 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0059-129.57 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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