D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.]

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  • D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.]

D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.]
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NDC 58264-0046-1
Set ID be8b4acb-83c6-4d25-ba90-ee6e6e0a588e
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 58264-0046-1

  • INDICATIONS

    Rheumatism, gout, swollen joints.

  • INGREDIENTS

    ACTIVE

    Ferrum phosphoricum 12x, Lithium carbonicum 12x, Natrum sulfuricum 30x, Nux vomica 30x, Rhododendron chrysanthum 6x, Spiraea ulmaria 12x

    INACTIVE

    20% alcohol in purified water.

  • Rx CAUTION

    Federal law prohibits dispensing without a prescription.

  • 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 46

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    D-46 
    ferrosoferric phosphate, lithium carbonate, sodium sulfate, strychnos nux-vomica seed, rhododendron aureum leaf, and filipendula ulmaria root solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0046
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Ferrosoferric phosphate (UNII: 91GQH8I5F7) (Ferrosoferric phosphate - UNII:91GQH8I5F7) Ferrosoferric phosphate12 [hp_X]  in 1 mL
    Lithium carbonate (UNII: 2BMD2GNA4V) (Lithium cation - UNII:8H8Z5UER66) Lithium carbonate12 [hp_X]  in 1 mL
    Sodium Sulfate (UNII: 0YPR65R21J) (Sodium sulfate anhydrous - UNII:36KCS0R750) Sodium Sulfate30 [hp_X]  in 1 mL
    Strychnos nux-vomica seed (UNII: 269XH13919) (Strychnos nux-vomica seed - UNII:269XH13919) Strychnos nux-vomica seed30 [hp_X]  in 1 mL
    Rhododendron Aureum Leaf (UNII: IV92NQJ73U) (Rhododendron Aureum Leaf - UNII:IV92NQJ73U) Rhododendron Aureum Leaf6 [hp_X]  in 1 mL
    Filipendula ulmaria root (UNII: 997724QNDS) (Filipendula ulmaria root - UNII:997724QNDS) Filipendula ulmaria root12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0046-129.57 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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