Bartonella Kit

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2022-08-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:54:40

Label at a glance#

ProductBartonella Kit
Active ingredientBARTONELLA BACILLIFORMIS, BARTONELLA CLARRIDGEIAE, BARTONELLA ELIZABETHAE, BARTONELLA HENSELAE, BARTONELLA QUINTANA, BARTONELLA VINSONII, BARTONELLA WASHOENSIS
Label structure9 sections

Dosage and administration

Adults take one vial orally every third day. Begin with vial #1 then vial #2 three days later, followed by each succeeding numbered vial in three day intervals. Consult your healthcare provider with any questions.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Bartonella Bacilliformis 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Clarridgeiae 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Elizabethae 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Henselae 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Quintana 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Vinsonii 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

Bartonella Washoensis 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms including slight fever, headache, chills, backache, and malaise.**


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

WARNINGS:

WARNINGS SECTION

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

If pregnant or nursing, seek the advice of a health professional before use.

If symptoms persist or recur, consult your health practitioner.

Symptoms often become acute between the second and fourth dose as part of the normal healing process.

It is recommended to continue Series Therapy until completion for best results.

Tamper seal: 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

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults take one vial orally every third day.

Begin with vial #1 then vial #2 three days later, followed by each succeeding numbered vial in three day intervals.

Consult your healthcare provider with any questions.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms including slight fever, headache, chills, backache, and malaise.**


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

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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

SERIES THERAPY

HOMEOPATHIC

BARTONELLA

FOR PROFESSIONAL USE ONLY

10 vials, 2 ml each

Bartonella Kit boxBartonella Kit box

Bartonella Kit vialBartonella Kit vial

Products#

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NDC Codes#

Ingredients#

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

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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
f42a00d7-8682-4b5e-b21c-a257bfcdacd220b4c53a-e0a1-4de2-8229-90d75047eb192022-08-31WarningsExact identifier
spl id: f42a00d7-8682-4b5e-b21c-a257bfcdacd2
spl set id: 20b4c53a-e0a1-4de2-8229-90d75047eb19

Reported adverse events (FAERS/openFDA)#

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