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.

HOMEOPATHIC INDICATIONS:

For temporary relief of skin rashes, general fatigue, craving for fruit, headaches, and indigestion.**

**These statements are based upon traditional homeopathic practice. 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:

For temporary relief of skin rashes, general fatigue, craving for fruit, headaches, and indigestion.**

**These statements are based upon traditional homeopathic practice. 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 DISPLAY LABEL:

DESBIO

NDC 43742-0659-1

HOMEOPATHIC

CINNAMIC ACID

1 FL OZ (30 ml)

Cinnamic Acid

CINNAMIC ACID
cinnamic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0659
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CINNAMIC ACID (UNII: U14A832J8D) (CINNAMIC ACID - UNII:U14A832J8D)	CINNAMIC ACID	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:43742-0659-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	11/11/2015	11/15/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		11/11/2015	11/15/2022

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0659) , api manufacture(43742-0659) , label(43742-0659) , pack(43742-0659)

Revised: 11/2018

Document Id: 49f58929-6623-4b62-9a05-0fc0ca5e67da

Set id: dde2dda5-f37c-45c9-ad99-4d6e50b13485

Version: 2

Effective Time: 20181106

Deseret Biologicals, Inc.