Caffeic Acid by Deseret Biologicals, Inc. / Apotheca Company CAFFEIC ACID liquid

Caffeic Acid by

Drug Labeling and Warnings

Caffeic Acid by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Caffeic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS

For temporary relief of sinus congestion, headache, indigestion, joint pains, dizziness, tingling nd numbness of extremities. 

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. 

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 physician or Poison Control Center right away.

INDICATIONS AND USAGE

For temporary relief of sinus congestion, headache, indigestion, joint pains, dizziness, tingling nd numbness of extremities.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-0219-1

HOMEOPATHIC

CAFFEIC ACID

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

CAFFEIC ACID 
caffeic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0219
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAFFEIC ACID (UNII: U2S3A33KVM) (CAFFEIC ACID - UNII:U2S3A33KVM)	CAFFEIC 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: 43742-0219-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/08/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/08/2013	05/27/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0219) , api manufacture(43742-0219) , label(43742-0219) , pack(43742-0219)