Dopamine

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company, Inc.
Effective date
2024-02-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:07

Label at a glance#

ProductDopamine
Active ingredientDOPAMINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • headache • reading difficulty • poor memory These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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

PURPOSE:

OTC - PURPOSE SECTION

Dopamine Hydrochloride - Headache, Reading Difficulty, Poor Memory

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• headache • reading difficulty • poor memory

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

Tamper Evident: Sealed for Your Protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

Dopamine

Homeopathic

NDC 43742-1281-1

1 FL OZ (30 ml)

DopamineDopamine

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6aba2aa6-bc33-4b0c-a81c-06f5fb4cc762Product name220180613
b2a69ae1-a082-5ec0-42b6-e3c38800f173Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1281-1Dopamine30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1281DOPAMINE (DOPAMINE HYDROCHLORIDE) LIQUID [DESERET BIOLOGICALS, INC.]2Current NDC, Legacy NDC, 1 package rows20240221_b984b509-cdeb-4fc9-8133-be3b7ba82c8c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-128143742-1281-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DOPAMINE HYDROCHLORIDE7L3E358N9LACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DopamineDOPAMINE HYDROCHLORIDEDeseret Biologicals, Inc.b984b509-cdeb-4fc9-8133-be3b7ba82c8c2024-02-20WarningsExact identifier
ndc (package): 43742-1281-1
ndc (product): 43742-1281
ndc11 (package): 43742128101
spl id: 1e29b059-a74a-48f1-b1b7-90ba47d6a311
spl set id: b984b509-cdeb-4fc9-8133-be3b7ba82c8c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.