FDA.reportPublic FDA data

Co-InfXn

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:55:51

Label at a glance#

ProductCo-InfXn
Active ingredientANAPLASMA PHAGOCYTOPHILUM, BABESIA MICROTI, BARTONELLA HENSELAE, BORRELIA BURGDORFERI, EHRLICHIA CANIS, MYCOPLASMA PNEUMONIAE, MEASLES VIRUS, NEISSERIA MENINGITIDIS, HEPATITIS B VIRUS
Label structure9 sections

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 INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Anaplasma Remedy 15X, 30X, 60X, 100X, 200X, Babesia Microti 15X, 30X, 60X, 100X, 200X, Bartonella Henselae 15X, 30X, 60X, 100X, 200X, Borrelia Burgdorferi Nosode 15X, 30X, 60X, 100X, 200X, Ehrlichia Nosode (Canine) 15X, 30X, 60X, 100X, 200X, Mycoplasma Pneumoniae 15X, 30X, 60X, 100X, 200X, Morbillinum 16X, 30X, 60X, 100X, 200X, Meningococcus Nosode 21X, 30X, 60X, 100X, 200X, Hepatitis B Nosode 15C, 30C, 60C, 100C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporarily relief of symptoms related to Lyme disease or other co-infections including joint pain, severe headaches, fever, severe muscle aches/pain, flu-like feelings of headache, stiff neck, muscle aches, and change in smell/taste, difficulty chewing, swallowing or speaking, hoarseness of vocal cord problems.**

**These statements are based upon traditional homeopathic practice. 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 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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a 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.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporarily relief of symptoms related to Lyme disease or other co-infections including joint pain, severe headaches, fever, severe muscle aches/pain, flu-like feelings of headache, stiff neck, muscle aches, and change in smell/taste, difficulty chewing, swallowing or speaking, hoarseness of vocal cord problems.**

**These statements are based upon traditional homeopathic practice. 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
NDC 43742-1570-1
HOMEOPATHIC
Co-InfXn
1 FL OZ (30 ml)

Co-InfXnCo-InfXn

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1570CO-INFXN (ANAPLASMA PHAGOCYTOPHILUM, BABESIA MICROTI, BARTONELLA HENSELAE, BORRELIA BURGDORFERI NOSODE, EHRLICHIA NOSODE (CANINE), MYCOPLASMA PNEUMONIAE, MORBILLINUM, MENINGOCOCCUS NOSODE, HEPATITIS B NOSODE) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210121_7f2ba436-804c-4128-b5e4-36a79d694c64.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-157043742-1570-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANAPLASMA PHAGOCYTOPHILUMBHE5668847ACTIB
BABESIA MICROTI1948X6KEG3ACTIB
BARTONELLA HENSELAE84PG7W9845ACTIB
BORRELIA BURGDORFERI0J8NV9V5Q8ACTIB
EHRLICHIA CANIS970Y8T1JZYACTIB
MYCOPLASMA PNEUMONIAEJQE470FAD0ACTIB
MEASLES VIRUSHT3R7C012QACTIB
NEISSERIA MENINGITIDISV3TP2MD7F3ACTIB
HEPATITIS B VIRUS77H9EM77P7ACTIB
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
47984cbf-e26a-429c-be77-cef142d816107f2ba436-804c-4128-b5e4-36a79d694c642021-01-20WarningsExact identifier
spl id: 47984cbf-e26a-429c-be77-cef142d81610
spl set id: 7f2ba436-804c-4128-b5e4-36a79d694c64

Reported adverse events (FAERS/openFDA)#

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