Adrenalinum by OHM PHARMA INC. ADRENALINUM pellet

Adrenalinum by

Drug Labeling and Warnings

Adrenalinum by is a Homeopathic medication manufactured, distributed, or labeled by OHM PHARMA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS: ACTIVE INGREDIENTS: ADRENALINUM

CONTENT: Approx. 100 Pellets

INDICATIONS & USAGE

USE: To be used according to standard homeopathic indications.

WARNINGS

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.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENTS: Organic sucrose, lactose free. 

QUESTIONS

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

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.

To be used according to standard homeopathic indications.

INGREDIENTS AND APPEARANCE

ADRENALINUM 
adrenalinum pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-778
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH)	EPINEPHRINE	6 [hp_C]  in 6 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66096-778-01	6 [hp_C] in 1 TUBE; Type 0: Not a Combination Product	11/01/2019

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

Labeler - OHM PHARMA INC. (030572478)