EMVITA 4- apis mellifica, oophorinum, platinum met, orchitinum, petroleum, stramonium liquid

Emvita 4 by

Drug Labeling and Warnings

Emvita 4 by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

​Drug Facts

​Active Ingredients: ​(HPUS*) 16.7% of each

Apis mellifica 21X     Orchitinum 21X

Oophorinum 21X       Petroleum 16LM

Platinum met 800C    Stramonium 18LM

*The letters "HPUS" indicate that the

components in this product are officially

monographed in the Homeopathic

Pharmacopoeia of the United States.

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

INDICATIONS & USAGE

​Uses: ​(†) Homepathic remedy for 

extreme self-control.

WARNINGS

​Warnings:

Stop use if symptoms persist or worsen.

​If you are pregnant or breastfeeding,

​consult a health care professional prior to use.

​Keep out of reach of children.

Keep out of reach of children.

INDICATIONS & USAGE

​Directions: ​(adults & children 6 years & older)

Take 5 drops 3 - 6 times daily, or as

recommended by your health care

professional.

OTHER SAFETY INFORMATION

​Other information: ​Store at 20 - 25ºC

(68 - 77ºF). Do not use if box has been

tampered with, or if safety seal of the bottle is broken.

INACTIVE INGREDIENT

​Inactive ingredients: ​Ethanol 20% USP,

Purified Water.

QUESTIONS

Manufactured by: OHM pharma, Inc., USA.

Distributed by: Privia Naturals, LLC.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

www.privianaturals.com

1 (888) 526-9695 Product of USA.

PRINCIPAL DISPLAY PANEL

​NDC: 66343-053-50

RUBIMED

Emvita 4

Homeopathic Medicine For

Extreme Self-Control

Homeopathic Medicine For

Extreme Self-Control

INGREDIENTS AND APPEARANCE

EMVITA 4 
apis mellifica, oophorinum, platinum met, orchitinum, petroleum, stramonium liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 66343-053
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	21 [hp_X]  in 50 mL
SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O)	SUS SCROFA OVARY	21 [hp_X]  in 50 mL
PLATINUM (UNII: 49DFR088MY) (PLATINUM - UNII:49DFR088MY)	PLATINUM	800 [hp_C]  in 50 mL
SUS SCROFA TESTICLE (UNII: KM02613O28) (SUS SCROFA TESTICLE - UNII:KM02613O28)	SUS SCROFA TESTICLE	21 [hp_X]  in 50 mL
KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E)	KEROSENE	16 [hp_M]  in 50 mL
DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3)	DATURA STRAMONIUM	18 [hp_M]  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-053-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/03/2019

Labeler - RUBIMED AG (480582035)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66343-053)