DRUG FACTS:

Drug Labeling and Warnings

Drug Details [pdf]

CINNAMIC ACID- cinnamic acid 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:

Cinnamic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of skin rashes, general fatigue, craving for fruit, headaches, indigestion, and high blood glucose levels.

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.

INDICATIONS:

For temporary relief of skin rashes, general fatigue, craving for fruit, headaches, indigestion, and high blood glucose levels.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070   www.desbio.com

PACKAGE DISPLAY LABEL:

​DESBIO

NDC: 43742-0296-1

HOMEOPATHIC

CINNAMIC ACID

1 FL OZ (30 ml)

CINNAMIC ACID 
cinnamic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0296
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CINNAMIC ACID (UNII: U14A832J8D) (CINNAMIC ACID - UNII:U14A832J8D)	CINNAMIC ACID	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-0296-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/30/2013	08/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/30/2013	08/26/2019

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0296) , api manufacture(43742-0296) , label(43742-0296) , pack(43742-0296)

Revised: 11/2018

Document Id: 0cc267ff-eb6b-4f82-8690-d7f23d176507

34390-5

Set id: 9c0dc2c1-6798-4e08-8627-aabd982aa829

Version: 2

Effective Time: 20181106