GABA- .gamma.-aminobutyric acid liquid 
Deseret Biologicals, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Drug Facts

ACTIVE INGREDIENTS:

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

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.

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.

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.

INACTIVE INGREDIENTS:

Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN.

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

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.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0178-1

HOMEOPATHIC

GABA

1 FL OZ (30 ml)

GABA

GABA 
gaba, liquid
Product Information
Product Type HUMAN OTC DRUG 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 (UNII: 2ACZ6IPC6I) (.GAMMA.-AMINOBUTYRIC ACID - UNII:2ACZ6IPC6I) .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
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)

Revised: 11/2012
Document Id: 76ea6403-860a-442b-8b64-ac046099486a
Set id: f9865bc1-2699-4cee-8a23-88ae4d7f8629
Version: 1
Effective Time: 20121107
 
Deseret Biologicals, Inc.