COUMARIN- coumarinum, 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:

Coumarinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of allergies caused by dairy products, foods, tobacco, wheat, bowel disorders including celiac disease, colitis, poor digestion, back and neck pain and asthma.

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.

INACTIVE INGREDIENTS:

For temporary relief of allergies caused by dairy products, foods, tobacco, wheat, bowel disorders including celiac disease, colitis, poor digestion, back and neck pain and asthma.

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.

KEEP OUT OF REACH OF CHILDREN:

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

INDICATIONS:

For temporary relief of allergies caused by dairy products, foods, tobacco, wheat, bowel disorders including celiac disease, colitis, poor digestion, back and neck pain and asthma.

QUESTIONS:

Dist. By:

Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0063-1

HOMEOPATHIC

COUMARIN

1 FL OZ (30 ml)

Coumarin

COUMARIN
coumarinum, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0063
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
COUMARIN (UNII: A4VZ22K1WT) (COUMARIN - UNII:A4VZ22K1WT)	COUMARIN	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:43742-0063-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	06/27/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		06/27/2012	12/19/2018

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0063) , api manufacture(43742-0063) , label(43742-0063) , pack(43742-0063)

Revised: 6/2016

Document Id: a34bdbb4-ece2-4911-89ea-95e6bdc982a4

Set id: 02d05771-f46d-405d-a7d7-b6e05a7572a7

Version: 3

Effective Time: 20160623

Deseret Biologicals, Inc.