FDA.reportPublic FDA data

Adrenalinum

Manufacturer
OHM PHARMA INC.
Effective date
2021-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:15:26

Label at a glance#

ProductAdrenalinum
Active ingredientEPINEPHRINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

DRUG FACTS: ACTIVE INGREDIENTS: ADRENALINUM

CONTENT: Approx. 100 Pellets

INDICATIONS & USAGE SECTION

USE: To be used according to standard homeopathic indications.

WARNINGS SECTION

WARNINGS: Keep out of reach of children. If pregnant or breast-feeding, ask a health care professional before use.  Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Dissolve 3-5 pellets under the tongue 3 times a day or as directed by professional.

OTHER SAFETY INFORMATION

OTHER INFORMATION: Store at room temperature.  Do not use if pellet dispenser seal is broken. 

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Organic sucrose, lactose free. 

OTC - QUESTIONS SECTION

Manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS).

PRODUCT OF USA. 

Mfg. By: OHM PHARMA, INC. Mineral Wells, TX 76067

www.ohmpharma.com FDA Est # 3003231743

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ADRENALINUM

The OTC Potency range from Adrenalinum 6X-30X, 3C-30C, 200C, 1M.

Standard bottle sizes for dilution-form can range from 30mL to 60mL.

MD Tube LabelMD Tube Label

OTC - PURPOSE SECTION

To be used according to standard homeopathic indications.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-778-01Adrenalinum6 [hp_C] in 1 TUBEPELLET63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-778ADRENALINUM PELLET [OHM PHARMA INC.]3Current NDC, Legacy NDC, 1 package rows20211230_a2a444fa-4337-42e3-bb31-2289c42f057e.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-77866096-778-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
EPINEPHRINEYKH834O4BHACTIB

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
AdrenalinumADRENALINUMOHM PHARMA INC.a2a444fa-4337-42e3-bb31-2289c42f057e2021-12-29WarningsExact identifier
ndc (package): 66096-778-01
ndc (product): 66096-778
ndc11 (package): 66096077801
spl id: d450922f-3861-3f22-e053-2995a90a9c7d
spl set id: a2a444fa-4337-42e3-bb31-2289c42f057e

Reported adverse events (FAERS/openFDA)#

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