EMVITA 13- bothrops atrox venom, oyster shell calcium carbonate, crude, graphite, anacardium occidentale fruit, and sus scrofa thymus liquid

Emvita 13 by

Drug Labeling and Warnings

Emvita 13 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: Feeling hurt

Ingredients

Bothrops 800 C
Calcarca carbonica 16 LM
Graphites 18 LM
Anacardium occ. 21 x
Thymus 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 13

Homeopathic Combination
Medicine Indications:
Feeling hurt

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 13 
bothrops atrox venom, oyster shell calcium carbonate, crude, graphite, anacardium occidentale fruit, and sus scrofa thymus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-025
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Bothrops Atrox Venom (UNII: K0Q6REZ9JC) (Bothrops Atrox Venom - UNII:K0Q6REZ9JC)	Bothrops Atrox Venom	800 [hp_C]  in 1 mL
Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I)	Oyster shell calcium carbonate, crude	16 [hp_M]  in 1 mL
Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O)	Graphite	18 [hp_M]  in 1 mL
Anacardium Occidentale Fruit (UNII: 4A10JR4E7E) (Anacardium Occidentale Fruit - UNII:4A10JR4E7E)	Anacardium Occidentale Fruit	21 [hp_X]  in 1 mL
Sus Scrofa Thymus (UNII: 7B69B0BD62) (Sus Scrofa Thymus - UNII:7B69B0BD62)	Sus Scrofa Thymus	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: 66343-025-50	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(66343-025)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-025)