EMVITA 7- lachesis muta venom, lycopodium clavatum spore, anacardium occidentale fruit, phosphorus, and sus scrofa adrenal gland liquid

Emvita 7 by

Drug Labeling and Warnings

Emvita 7 by is a Otc medication manufactured, distributed, or labeled by RUBIMED AG, Omida AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Homeopathic Combination Medicine Indications: Defiance

Ingredients

Lachesis mutus 800 C
Lycopodium 16 LM
Anacard occ. 18 LM
Phosphorus 2l x
Glandula supra. 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 7

Homeopathic Combination
Medicine Indications:
Defiance

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 7 
lachesis muta venom, lycopodium clavatum spore, anacardium occidentale fruit, phosphorus, and sus scrofa adrenal gland liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-019
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Lachesis Muta Venom (UNII: VSW71SS07I) (Lachesis Muta Venom - UNII:VSW71SS07I)	Lachesis Muta Venom	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
Anacardium Occidentale Fruit (UNII: 4A10JR4E7E) (Anacardium Occidentale Fruit - UNII:4A10JR4E7E)	Anacardium Occidentale Fruit	18 [hp_M]  in 1 mL
Phosphorus (UNII: 27YLU75U4W) (Phosphorus - UNII:27YLU75U4W)	Phosphorus	21 [hp_X]  in 1 mL
Sus Scrofa Adrenal Gland (UNII: 398IYQ16YV) (Sus Scrofa Adrenal Gland - UNII:398IYQ16YV)	Sus Scrofa Adrenal Gland	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: 66343-019-50	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(66343-019)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-019)