Label: GABA- .gamma.-aminobutyric acid liquid 

  • Label RSS
  • NDC Code(s): 43742-0178-1
  • Packager: Deseret Biologicals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/12

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS:

    Gaba 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

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  • INDICATIONS:

    For temporary relief of symptoms related to Gaba sensitivity including hypertension, anger, hostility, Seasonal Affective Disorder, sleep difficulties, fatigue, depression, food sensitivities and sleep disorders.

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  • 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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  • 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 INGREDIENTS:

    Demineralized water, 25% Ethanol.

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  • KEEP OUT OF REACH OF CHILDREN.

    In case of overdose, contact physician or Poison Control Center right away.

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  • INDICATIONS:

    For temporary relief of symptoms related to Gaba sensitivity including hypertension, anger, hostility, Seasonal Affective Disorder, sleep difficulties, fatigue, depression, food sensitivities and sleep disorders.

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  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070

    www.desbio.com

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  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0178-1

    HOMEOPATHIC

    GABA

    1 FL OZ (30 ml)

    GABA

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  • INGREDIENTS AND APPEARANCE
    GABA 
    gaba, liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:43742-0178
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    .GAMMA.-AMINOBUTYRIC ACID (.GAMMA.-AMINOBUTYRIC ACID) .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0178-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 11/07/2012
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0178)
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