TOXO HOMO- toxoplasma gondii dna liquid

TOXO HOMO by

Drug Labeling and Warnings

TOXO HOMO by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Toxoplasma Gondii DNA 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X.

PURPOSE:

Toxoplasma Gondii DNA - Body Aches, Headache, Fever, Fatigue

USES:

For the temporary relief of symptoms including:

 body aches  headache  fever  fatigue 

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

WARNINGS:

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:

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

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

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

DesBio

TOXO:HOMO

Homeopathic

NDC: 43742-2002-1

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

TOXO HOMO 
toxoplasma gondii dna liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-2002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOXOPLASMA GONDII DNA (UNII: JMX3ACIU25) (TOXOPLASMA GONDII DNA - UNII:JMX3ACIU25)	TOXOPLASMA GONDII DNA	15 [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: 43742-2002-1	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/21/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-2002) , api manufacture(43742-2002) , label(43742-2002) , pack(43742-2002)