CANDIDA- candida albicans 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:

Candida Albicans 200C.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to Candida Albicans infection including nausea, drowsiness, lethargy, confusion, vertigo, vaginal discharge, sensitivities to foods and other fungi, petrochemicals, sleep disorders, mucous congestion and tinnitus.**

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

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.

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.

HOMEOPATHIC INDICATIONS:

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

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0091-1

HOMEOPATHIC

CANDIDA 200C

1 FL OZ (30 ml)

Candida 200C

CANDIDA
candida albicans liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0091
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	200 [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:43742-0091-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	01/07/2016	02/16/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/22/2012	02/16/2021

Labeler - Deseret Biologicals, Inc (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0091) , api manufacture(43742-0091) , label(43742-0091) , pack(43742-0091)

Revised: 4/2017

Document Id: 6c0c29a4-679c-4040-84cc-bd53a016bea5

Set id: 87e83b02-3b90-4afb-9f1f-cd4d98f16ae3

Version: 5

Effective Time: 20170406

Deseret Biologicals, Inc