EPSTEIN-BARR VIRUS REMEDY- epstein-barr virus nosode liquid
Deseret Biologicals, Inc.

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:

Epstein-Barr Virus Nosode 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

INDICATIONS:

For temporary relief of symptoms related to Epstein-Barr Virus including exhaustion, liver pain, swollen glands, mucous congestion, and fatigue.

WARNINGS:

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

If pregnant or breast-feeding, ask 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:

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

INDICATIONS AND USAGE:

For temporary relief of symptoms related to Epstein-Barr Virus including exhaustion, liver pain, swollen glands, mucous congestion, and fatigue.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0192-1

HOMEOPATHIC

EPSTEIN-BARR
VIRUS REMEDY

1 FL OZ (30 ml)

Epstein-Barr Virus Remedy

EPSTEIN-BARR VIRUS REMEDY
epstein-barr virus nosode liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0192
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (HUMAN HERPESVIRUS 4 - UNII:2A26YW7PNX)	HUMAN HERPESVIRUS 4	15 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0192-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		10/29/2012	07/30/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0192) , api manufacture(43742-0192) , label(43742-0192) , pack(43742-0192)

Revised: 3/2016

Document Id: a346ba10-1408-434e-a405-5363357992bc

Set id: a0891200-bb66-4549-a6b3-59646148583f

Version: 3

Effective Time: 20160308

Deseret Biologicals, Inc.