Octopamine

Manufacturer: BioActive Nutritional, Inc. | Apotheca Company
Effective date: 2023-08-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:26:50

Label at a glance#

ProductOctopamine

Active ingredientOCTOPAMINE HYDROCHLORIDE

Label structure9 sections

Dosage and administration

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Octopamine (Hydrochloride) 6X, 12X, 30X, 12C, 30C.

INDICATIONS:

OTC - PURPOSE SECTION

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

WARNINGS:

WARNINGS SECTION

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

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

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

OCTOPAMINE

HOMEOPATHIC

1 FL OZ (30 ml)

Octopamine

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43857-0503-1	2023-08-25	C162847	48780-1	ba0f9c33-4cf7-a910-e053-dadaa90a0b85	Drug Facts:
43857-0503-1	2021-01-29	C162847	48780-1	ba0f9c33-4cf7-a910-e053-dadaa90a0b85	Drug Facts:

Products#

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

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

Octopamine
Octopamine Hydrochloride
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43857-0503	43857-0503-1

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
Name	UNII	Kind
OCTOPAMINE HYDROCHLORIDE	37YAS5L9HQ	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
92b732e2-0397-4f11-9860-3c1206016bd0			77efc2ee-a59f-4bb2-956b-82762fe256a8	2023-08-25	Warnings	Exact identifier spl id: 92b732e2-0397-4f11-9860-3c1206016bd0 spl set id: 77efc2ee-a59f-4bb2-956b-82762fe256a8

Reported adverse events (FAERS/openFDA)#

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