EMVITA 9- lycopodium clavatum spore, lycosa tarantula, sulfur, calcium sulfide, and sus scrofa pancreas liquid

Emvita 9 by

Drug Labeling and Warnings

Emvita 9 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: Repressed emotions

Ingredients

Lycopodium 800 C
Tarantula hispana 16 LM
Sulphur 18 LM
Hepar sulphuris 21 x
Pancreas suis 2l 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 9

Homeopathic Combination
Medicine Indications:
Repressed emotions

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 9 
lycopodium clavatum spore, lycosa tarantula, sulfur, calcium sulfide, and sus scrofa pancreas liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-021
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	800 [hp_C]  in 1 mL
LYCOSA TARANTULA (UNII: 86M454L2TT) (LYCOSA TARANTULA - UNII:86M454L2TT)	LYCOSA TARANTULA	16 [hp_M]  in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	18 [hp_M]  in 1 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	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: 66343-021-50	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(66343-021)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-021)