CAN1 PC- 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 1M.

HOMEOPATHIC INDICATIONS:

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

**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 a 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.

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.

HOMEOPATHIC INDICATIONS:

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

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 43742-1741-1

HOMEOPATHIC

CAND1:PC

1 FL OZ (30ml)

CAND1:PC

CAN1 PC
candida albicans liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-1741
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	1 [hp_M] 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:43742-1741-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/12/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/12/2021

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-1741) , api manufacture(43742-1741) , label(43742-1741) , pack(43742-1741)

Revised: 1/2023

Document Id: d4c66e4e-13ef-41cd-ab4a-5cf7c0277c69

Set id: e208907f-90cd-4ab4-8437-c2dd654e9450

Version: 2

Effective Time: 20230113

Deseret Biologicals, Inc.