EMVITA 26- arsenic trioxide, lycopodium clavatum spore, lead, achillea millefolium, and sus scrofa cerebellum liquid

Emvita 26 by

Drug Labeling and Warnings

Emvita 26 by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG, Omida AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Homeopathic Combination Medicine Indications: Materialistic behavior

Ingredients

Arsenicum alb. 800 C
Lycopodium cl. 16 LM
Plumbum met. 18 LM
Millefolium 21 x
Cerebellum suis 21 x
Alcohol 38 % 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 26

Homeopathic Combination
Medicine Indications:
Materialistic behavior

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 26 
arsenic trioxide, lycopodium clavatum spore, lead, achillea millefolium, and sus scrofa cerebellum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-038
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Arsenic trioxide (UNII: S7V92P67HO) (Arsenic Cation (3+) - UNII:C96613F5AV)	Arsenic trioxide	800 [hp_C]  in 1 mL
Lycopodium clavatum spore (UNII: C88X29Y479) (Lycopodium clavatum spore - UNII:C88X29Y479)	Lycopodium clavatum spore	16 [hp_M]  in 1 mL
Lead (UNII: 2P299V784P) (Lead - UNII:2P299V784P)	Lead	18 [hp_M]  in 1 mL
Achillea Millefolium (UNII: 2FXJ6SW4PK) (Achillea Millefolium - UNII:2FXJ6SW4PK)	Achillea Millefolium	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

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)	0.38 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-038-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

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

Labeler - RUBIMED AG (480582035)

Establishment
Name	Address	ID/FEI	Business Operations
RUBIMED AG		480582035	MANUFACTURE(66343-038)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-038)