ADRENALINUM- adrenalinum pellet 
OHM PHARMA 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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Adrenalinum

DRUG FACTS: ACTIVE INGREDIENTS: ADRENALINUM

CONTENT: Approx. 100 Pellets

USE: To be used according to standard homeopathic indications.

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.

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

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

INACTIVE INGREDIENTS: Organic sucrose, lactose free. 

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

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 Label

To be used according to standard homeopathic indications.

ADRENALINUM 
adrenalinum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-778
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE6 [hp_C]  in 6 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScore    
ShapeROUNDSize4mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66096-778-016 [hp_C] in 1 TUBE; Type 0: Not a Combination Product11/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic11/01/2019
Labeler - OHM PHARMA INC. (030572478)

Revised: 12/2021
Document Id: d450922f-3861-3f22-e053-2995a90a9c7d
Set id: a2a444fa-4337-42e3-bb31-2289c42f057e
Version: 3
Effective Time: 20211229
 
OHM PHARMA INC.