D-100 (FUCUS VESICULOSUS) SOLUTION [DNA LABS, INC.]

  • Home
  • D-100 (FUCUS VESICULOSUS) SOLUTION [DNA LABS, INC.]

D-100 (FUCUS VESICULOSUS) SOLUTION [DNA LABS, INC.]
PDF | XML
NDC 58264-0106-1
Set ID 0a2aed6f-6e1c-43e4-b5df-1dc73d7e6f2b
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
View All SectionsClose All Sections
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0106-1

    Close
  • INDICATIONS

    Mental dullness, tremors, sweating.

    Close
  • INGREDIENTS

    ACTIVE

    Fucus vesiculosus 3/6/30x

    INACTIVE

    20% alcohol in purified water.

    Close
  • SUGGESTED DOSAGE

    One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

    Close
  • STORAGE AND HANDLING

    SHAKE WELL

    Close
  • 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.
    Close
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

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

    DYNAMIC
    NUTRITIONAL
    ASSOCIATES, INC.

    D 100

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
    Close
  • INGREDIENTS AND APPEARANCE
    D-100 
    fucus vesiculosus solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0106
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Fucus vesiculosus (UNII: 535G2ABX9M) (Fucus vesiculosus - UNII:535G2ABX9M) Fucus vesiculosus 3 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58264-0106-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    UNAPPROVED HOMEOPATHIC 01/01/1990
    Labeler - DNA Labs, Inc. (031784339)
    Close
View All SectionsClose All Sections

Related Drugs

Search DailyMed Drugs