EMVITA 10- calcium sulfide, lachesis muta venom, arisaema triphyllum root, kerosene, chaste tree, and sus scrofa pancreas liquid

Emvita 10 by

Drug Labeling and Warnings

Emvita 10 by is a Otc medication manufactured, distributed, or labeled by RUBIMED AG, Omida AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Homeopathic Combination Medicine Indications: Unfulfilled desires

Ingredients

Hepar sulphuris 800 C
Lachesis mutus 16 LM
Arum triph. 18 LM
Petroleum 21 x
Agnus castus 21 x
Pancreas Suis 21 x
Alcohol 40 % 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 10

Homeopathic Combination
Medicine Indications:
Unfulfilled desires

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 10 
calcium sulfide, lachesis muta venom, arisaema triphyllum root, kerosene, chaste tree, and sus scrofa pancreas liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-022
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	800 [hp_C]  in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	16 [hp_M]  in 1 mL
ARISAEMA TRIPHYLLUM ROOT (UNII: DM64K844DM) (ARISAEMA TRIPHYLLUM ROOT - UNII:DM64K844DM)	ARISAEMA TRIPHYLLUM ROOT	18 [hp_M]  in 1 mL
KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E)	KEROSENE	21 [hp_X]  in 1 mL
CHASTE TREE (UNII: 433OSF3U8A) (CHASTE TREE - UNII:433OSF3U8A)	CHASTE TREE	21 [hp_X]  in 1 mL
SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY)	SUS SCROFA PANCREAS	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: 66343-022-50	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(66343-022)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-022)