DOPAMINE- dopamine hydrochloride 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:

Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS:

For temporary relief of symptoms including arrhythmia, anxiety, depression, headache, reading difficulty, trembling of limbs, and poor memory.

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.

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 including arrhythmia, anxiety, depression, headache, reading difficulty, trembling of limbs, and poor memory.

QUESTIONS:

Dist By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070 www.desbio.com

Package Label Display:

DESBIO

NDC 43742-0403-1

HOMEOPATHIC

DOPAMINE

1 FL OZ (30 ml)

Dopamine

DOPAMINE
dopamine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0403
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L) (DOPAMINE - UNII:VTD58H1Z2X)	DOPAMINE HYDROCHLORIDE	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:43742-0403-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	03/14/2014	08/05/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		03/14/2014	08/05/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca, Inc. (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company, Inc.		844330915	manufacture(43742-0403) , api manufacture(43742-0403) , label(43742-0403) , pack(43742-0403)

Revised: 10/2018

Document Id: adfbaa11-9615-4455-b1c3-885962f9614c

Set id: 64d8e280-2801-4450-a23b-8ffe5980a456

Version: 2

Effective Time: 20181025

Deseret Biologicals, Inc.