T-38 (SALIX ALBA WHOLE) SOLUTION [DNA LABS, INC.]

  • Home
  • T-38 (SALIX ALBA WHOLE) SOLUTION [DNA LABS, INC.]

T-38 (SALIX ALBA WHOLE) SOLUTION [DNA LABS, INC.]
PDF | XML
NDC 58264-0283-1
Set ID a12994c7-e093-463a-b35c-4206b9197582
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
View All Sections
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0283-1

  • INDICATIONS

    Resentment, bitterness.

  • INGREDIENTS

    ACTIVE

    Salix vitellina 6/8/30x

    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.

    T-38
    WILLOW

    FLOWER ESSENCES

    1 FL. OZ.

    Principal Display Panel - 1 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    T-38 
    salix alba whole solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0283
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALIX ALBA WHOLE (UNII: V8UV0R324S) (SALIX ALBA WHOLE - UNII:V8UV0R324S) SALIX ALBA WHOLE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0283-129.57 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)
View All Sections

Related Drugs

Search DailyMed Drugs