EMVITA 8- ammonium carbonate, graphite, quinine arsenite, opium, and oyster shell calcium carbonate, crude liquid

Emvita 8 by

Drug Labeling and Warnings

Emvita 8 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 preparation for general well-being: Feeling isolated

Ingredients

Ammonium carb. 800 C
Graphites 166 IA
Chininum ars. 18 LM
Opium 21 x
Calcarea carbonica 21 x
Pancreas 21 x
Alcohol 40 % v/v

TAMPER-EVIDENT

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

Directions

10 drops per day or as instructed by your health care provider.

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 8

Homeopathic preparation
for general well-being:
Feeling isolated

RUBIMED®

1.7 Fl.oz. (50 ml)

INGREDIENTS AND APPEARANCE

EMVITA 8 
ammonium carbonate, graphite, quinine arsenite, opium, and oyster shell calcium carbonate, crude liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-020
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ammonium carbonate (UNII: NJ5VT0FKLJ) (Ammonium cation - UNII:54S68520I4, Carbonate ion - UNII:7UJQ5OPE7D)	Ammonium carbonate	800 [hp_C]  in 1 mL
Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O)	Graphite	16 [hp_M]  in 1 mL
Quinine arsenite (UNII: 42QO5P0NLM) (Quinine - UNII:A7V27PHC7A, Arsenite ion - UNII:N5509X556J)	Quinine arsenite	18 [hp_M]  in 1 mL
Opium (UNII: 37M3MZ001L) (Opium - UNII:37M3MZ001L)	Opium	21 [hp_X]  in 1 mL
Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I)	Oyster shell calcium carbonate, crude	21 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)	0.4 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-020-50	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(66343-020)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-020)