EMVITA 27- anacard occ, calcarea carbonica, cerebrum, helleborus niger, mandragora liquid

Emvita 27 by

Drug Labeling and Warnings

Emvita 27 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*) 20% of each

Anacard occ 18LM  Calcarea carbonica 21X
Cerebrum 21X       Helleborus niger 800C
Mandragora 16LM

*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: (†) Homeopathic remedy for general well being: inability to face reality.

WARNINGS

Warnings:

Stop use if symptoms persist or worsen.

If you are pregnant or breastfeeding, consult a healthcare professional prior to use. 

Keep out of reach of children. 

DOSAGE & ADMINISTRATION

Directions: (adults & children 6 years & older)

Take 12 drops 2 times daily, or as recommended by your health care professional. 

OTHER SAFETY INFORMATION

Other information: Store at 20 - 25°C

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

tampered with, or if the 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.

9169 W State St #196

Garden City, ID 83714

www.privianaturals.com

Info@privianaturals.com Product of USA.

PRINCIPAL DISPLAY PANEL

NDC: 66343-114-60

RUBIMED

Emvita 27

Homeopathic Medicine For

General Well-being: Inability To

Face Reality

2.0 fl oz. 59mL 20% Ethanol

Homeopathic Medicine For

General Well-being: Inability To

Face Reality

INGREDIENTS AND APPEARANCE

EMVITA 27 
anacard occ, calcarea carbonica, cerebrum, helleborus niger, mandragora liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-114
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E)	ANACARDIUM OCCIDENTALE FRUIT	18 [hp_M]  in 60 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	21 [hp_X]  in 60 mL
SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532)	SUS SCROFA CEREBRUM	21 [hp_X]  in 60 mL
HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815)	HELLEBORUS NIGER ROOT	800 [hp_C]  in 60 mL
MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB)	MANDRAGORA OFFICINARUM ROOT	16 [hp_M]  in 60 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: 66343-114-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/23/2022

Labeler - RUBIMED AG (480582035)