BRUCELLA REMEDY- brucella melitensis liquid 
Deseret Biologicals

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:

BRUCELLA MELITENSIS 11C, 15C, 30C, 45C, 60C, 75C, 100C, 250C, 500C

INDICATIONS:

FOR TEMPORARY RELIEF OF SYMPTOMS RELATED TO BRUCELLA INFECTION INCLUDING CHRONIC FATIGUE SYNDROME, FIBROMYALGIA, FEVER, SWEATS, MALAISE, ANOREXIA, HEADACHE, BACK PAIN, NECK PAIN, MALODOROUSE SWEAT, PECTULIAR TASTE IN MOUTH, AND GUT INFLAMMATION.

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 BRUCELLA INFECTION INCLUDING CHRONIC FATIGUE SYNDROME, FIBROMYALGIA, FEVER, SWEATS, MALAISE, ANOREXIA, HEADACHE, BACK PAIN, NECK PAIN, MALODOROUSE SWEAT, PECTULIAR TASTE IN MOUTH, AND GUT INFLAMMATION.

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070 www.desbio.com

DESBIO

NDC 43742-0163-1

HOMEOPATHIC

BRUCELLA REMEDY

1 FL OZ (30 ML)

BRUCELLA REMEDY

BRUCELLA REMEDY 
brucella melitensis liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0163
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRUCELLA MELITENSIS (UNII: OQF85710LZ) (BRUCELLA MELITENSIS - UNII:OQF85710LZ) BRUCELLA MELITENSIS 11 [hp_C]  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:43742-0163-1 30 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 09/28/2012
Labeler - Deseret Biologicals (940741853)
Registrant - Apotheca Company (844330915)
Establishment
Name Address ID/FEI Business Operations
Apotheca Company 844330915 manufacture(43742-0163)

Revised: 9/2012
Document Id: 769898ec-3aa0-493a-83dd-e33a0d6e40d7
Set id: fe3eb1d3-205a-445a-a2ac-dcab56f3357e
Version: 1
Effective Time: 20120928
 
Deseret Biologicals