Octopamine by Deseret Biologicals, Inc. / Apotheca Company DRUG FACTS:

Octopamine by

Drug Labeling and Warnings

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

Drug Details [pdf]

OCTOPAMINE- octopamine 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:

Octopamine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS:

For temporary relief of headaches, indigestion, heavy chest, burning pain in left arm, and mental sluggishness.

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.

INDICATIONS:

For temporary relief of headaches, indigestion, heavy chest, burning pain in left arm, and mental sluggishness.

INACTIVE INGREDIENTS:

Demineralized Water, Ethanol 25%

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070    www.desbio.com

PACKAGE DISPLAY LABEL:

​DESBIO

NDC: 43742-0304-1

HOMEOPATHIC

​OCTOPAMINE

​1 FL OZ (30 ml)

OCTOPAMINE 
octopamine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0304
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOPAMINE (UNII: 14O50WS8JD) (OCTOPAMINE - UNII:14O50WS8JD)	OCTOPAMINE	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: 43742-0304-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	01/10/2014	11/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/10/2014	11/26/2019

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0304) , api manufacture(43742-0304) , label(43742-0304) , pack(43742-0304)

Revised: 4/2018

Document Id: 61f2c44d-f7c7-4a95-82df-742802dd2663

34390-5

Set id: aea30147-9167-40b8-83cf-f7c2a2ff80d8

Version: 2

Effective Time: 20180413

 

Deseret Biologicals, Inc.