EMVITA 28- mandragora officinarum root, helleborus niger root, hyoscyamus niger, and sus scrofa cerebellum liquid
RUBIMED AG

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.

----------

Emvita 28

Homeopathic Combination Medicine Indications: Jugdemental behavior

Ingredients

Mandragora 800 C
Helleborus niger 18 LM
Hyoscyamus niger 21 x
Cerebellum suis 21 x
Alcohol 43 % v/v

TAMPER-EVIDENT

Do not use this product if seal at base of cap is missing or broken.

Direction

12 drops two times per day or as directed by the practitioner.

Warnings

As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using the product.

Keep out of Reach of Children!

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

Emvita 28

Homeopathic Combination
Medicine Indications:
Judgemental behaviour

RUBIMED®

1.7 Fl.oz. (50ml)

Principal Display Panel - 50 ml Bottle Label

EMVITA 28
mandragora officinarum root, helleborus niger root, hyoscyamus niger, and sus scrofa cerebellum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66343-040
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB)	MANDRAGORA OFFICINARUM ROOT	800 [hp_C] in 1 mL
HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815)	HELLEBORUS NIGER ROOT	18 [hp_M] in 1 mL
HYOSCYAMUS NIGER (UNII: 4WRK2153H3) (HYOSCYAMUS NIGER - UNII:4WRK2153H3)	HYOSCYAMUS NIGER	21 [hp_X] in 1 mL
SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (SUS SCROFA CEREBELLUM - UNII:49NGK53TPQ)	SUS SCROFA CEREBELLUM	21 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Alcohol (UNII: 3K9958V90M)	0.43 mL in 1 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66343-040-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
UNAPPROVED HOMEOPATHIC		05/07/2015

Labeler - RUBIMED AG (480582035)

Name	Address	ID/FEI	Business Operations
Establishment
RUBIMED AG		480582035	MANUFACTURE(66343-040)

Name	Address	ID/FEI	Business Operations
Establishment
Omida AG		483268348	MANUFACTURE(66343-040)