PHENYL ISOTHIOCYANATE- phenyl isothiocyanate 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:

Phenyl Isothiocyanate 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of symptoms of gastro-intestinal distress as in colitis or diarrhea, cardiovascular irregularities, hypertension, and thyroid dysfunction.

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.

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 a physician or Poison Control Center right away.

INDICATIONS:

For temporary relief of symptoms of gastro-intestinal distress as in colitis or diarrhea, cardiovascular irregularities, hypertension, and thyroid dysfunction.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0222-1

HOMEOPATHIC

PHENYL

ISOTHIOCYANATE

1 FL OZ (30 ml)

Phenyl Isothiocyanate

PHENYL ISOTHIOCYANATE
phenyl isothiocyanate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0222
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PHENYL ISOTHIOCYANATE (UNII: 0D58F84LSU) (PHENYL ISOTHIOCYANATE - UNII:0D58F84LSU)	PHENYL ISOTHIOCYANATE	6 [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:43742-0222-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/12/2013	05/28/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/12/2013	05/28/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0222) , api manufacture(43742-0222) , label(43742-0222) , pack(43742-0222)

Revised: 3/2018

Document Id: 7395e493-eac7-48d5-b87d-e14055dee372

Set id: 0313225e-dbe0-47a8-bbfd-275d21f82d11

Version: 3

Effective Time: 20180316

Deseret Biologicals, Inc.