BIOLOGICAL COMPLEX I- variolinum 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.

----------

DRUG FACTS:

ACTIVE INGREDIENTS:

Variolinum 30C.

INDICATIONS:

For temporary relief of symptoms related to Smallpox biological substance exposure.

WARNINGS:

Keep out of reach of children. In case of overdose, contact 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:

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

DIRECTIONS:

1-10 drops under the tongue, 3 times daily for 1 week. Wait 3 weeks and then repeat the first weeks dosage or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of symptoms related to Smallpox biological substance exposure.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

DIST. BY:

Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0002-1

HOMEOPATHIC

BIOLOGICAL

COMPLEX I

1 FL OZ (30 ml)

Biological Complex I

BIOLOGICAL COMPLEX I
variolinum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0002
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN - UNII:4SV59689SK)	VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN	30 [hp_C] 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:43742-0002-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	06/21/2014	03/11/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		06/21/2014	03/11/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0002) , api manufacture(43742-0002) , label(43742-0002) , pack(43742-0002)

Revised: 3/2018

Document Id: 0eecb5c5-c8fb-4b11-a751-c2ce92306bfc

Set id: bfed1c0d-eb2a-46b4-935a-6a432de6befe

Version: 2

Effective Time: 20180307

Deseret Biologicals, Inc.