CONDYLOMATA REMEDY- human papilloma 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:

Human papillomavirus 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X.

INDICATIONS:

For the temporary relief of symptoms related to Human Papilloma Virus including genital warts, itching in pelvic area and bleeding during intercourse.

WARNINGS:

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.

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.

INDICATIONS:

For the temporary relief of symptoms related to Human Papilloma Virus including genital warts, itching in pelvic area and bleeding during intercourse.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0339-1

HOMEOPATHIC

CONDYLOMATA REMEDY

1 FL OZ (30 ml)

Condylomata Remedy

CONDYLOMATA REMEDY
human papilloma nosode, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0339
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (HUMAN PAPILLOMAVIRUS - UNII:23CVL7WF4J)	HUMAN PAPILLOMAVIRUS	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:43742-0339-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	06/21/2014	11/17/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		06/21/2014	11/17/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0339) , api manufacture(43742-0339) , label(43742-0339) , pack(43742-0339)

Revised: 10/2016

Document Id: 1ecc2838-059a-465e-be68-a9fecec2b9ef

Set id: bd5d55f4-3ae1-4a4c-861a-91b54a02f0f2

Version: 2

Effective Time: 20161021

Deseret Biologicals, Inc.