BRUC HOMO

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-04-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:26:43

Label at a glance#

ProductBRUC HOMO
Active ingredientBRUCELLA MELITENSIS
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • fever • sweats • malaise • headache • back pain • neck pain • malodorous sweat • gut inflammation These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Brucella Melitensis 18C, 24C, 30C, 45C, 60C, 75C, 100C, 250C, 500C.

PURPOSE:

OTC - PURPOSE SECTION

Brucella Melitensis - Fever, Sweats, Malaise, Headache, Back Pain, Neck Pain, Malodorous Sweat, Gut Inflammation

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• fever • sweats • malaise • headache • back pain

• neck pain • malodorous sweat • gut inflammation

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

BRUC:HOMO

Homeopathic

NDC 43742-1729-1

1 FL OZ (30 ml)

BRUC:HOMOBRUC:HOMO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1729-1BRUC HOMO30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1729BRUC HOMO (BRUCELLA MELITENSIS) LIQUID [DESERET BIOLOGICALS, INC.]3Current NDC, Legacy NDC, 1 package rows20240425_916e818d-3f85-4020-ae9b-755d348576be.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-172943742-1729-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BRUCELLA MELITENSISOQF85710LZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BRUC HOMOBRUCELLA MELITENSISDeseret Biologicals, Inc.916e818d-3f85-4020-ae9b-755d348576be2024-04-23WarningsExact identifier
ndc (package): 43742-1729-1
ndc (product): 43742-1729
ndc11 (package): 43742172901
spl id: d09f61f8-b7f4-49be-bcb5-e2e5353beb80
spl set id: 916e818d-3f85-4020-ae9b-755d348576be

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.