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 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms including headache, reading difficulty, and poor memory.**

**These statements are based upon homeopathic principles. 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 symptoms including headache, reading difficulty, and poor memory.**

**These statements are based upon homeopathic principles. 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 LABEL DISPLAY:

DESBIO

NDC 43742-1281-1

HOMEOPATHIC

DOPAMINE

1 FL OZ (30 ml)

Dopamine

DOPAMINE 
dopamine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-1281
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L) (DOPAMINE - UNII:VTD58H1Z2X) DOPAMINE HYDROCHLORIDE8 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-1281-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/27/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/27/2018
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company, Inc. (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company, Inc.844330915manufacture(43742-1281) , api manufacture(43742-1281) , label(43742-1281) , pack(43742-1281)

Revised: 7/2018
Document Id: 8cf752d8-1148-4807-87ad-730c6a6270cb
Set id: b984b509-cdeb-4fc9-8133-be3b7ba82c8c
Version: 1
Effective Time: 20180727
 
Deseret Biologicals, Inc.