Available Formats

• ACTIVE INGREDIENT

  ACTIVE INGREDIENTS:  Taurine  6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.
  

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• PURPOSE

  INDICATIONS:  For temporary relief of symptoms related to toxicity from petrochemicals, pesticides, foods, environmental toxins including angina, autism, obsessive/compulsive behavior, fatigue, foggy brain, poor concentration, retinal dysfunction, headache, nasal and sinus congestion.
  

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• WARNINGS

  WARNINGS:  Keep out of reach of children.  in case of overdose, contact physician or Poison Control Center right away.

  If pregnant or breast-feeding, seek advice of a health professional before use.

  Tamper seal:  "Sealed for Your Protection."  Do not use if seal is broken or missing.
  

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• DOSAGE & ADMINISTRATION

  DIRECTIONS:  1-10 drops under the tongue, 3 times a day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.
  

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• INACTIVE INGREDIENT

  INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.
  

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• KEEP OUT OF REACH OF CHILDREN

  KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.
  

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• INDICATIONS & USAGE

  INDICATIONS:  For temporary relief of symptoms related to toxicity from petrochemicals, pesticides, foods, environmental toxins including angina, autism, obsessive/compulsive behavior, fatigue, foggy brain, poor concentration, retinal dysfunction, headache, nasal and sinus congestion.
  

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• QUESTIONS

  Dist. By:

  Deseret Biologicals, Inc.

  469 Parkland Drive

  Sandy, UT 84070

  www.desbio.com

  
  

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• PRINCIPAL DISPLAY PANEL

  DESBIO

  NDC 43742-0058-1

  HOMEOPATHIC

  TAURINE

  1 FL OZ (30 ml)

  

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• INGREDIENTS AND APPEARANCE

  TAURINE  taurine, liquid

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0058 Route of Administration ORAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAURINE (UNII: 1EQV5MLY3D) (TAURINE - UNII:1EQV5MLY3D) TAURINE 6 [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:43742-0058-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 06/04/2012 09/18/2020

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/04/2012 09/18/2020

  Labeler - Deseret Biologicals, Inc. (940741853)

  Registrant - Apotheca Company (844330915)

  Establishment
  Name	Address	ID/FEI	Business Operations
  Apotheca Company		844330915	manufacture(43742-0058)

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