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

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

Emvita 9

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)

Principal Display Panel - 50 ml Bottle Label

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66343-021-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
Unapproved homeopathic		05/07/2015

Labeler - RUBIMED AG (480582035)

Name	Address	ID/FEI	Business Operations
Establishment
RUBIMED AG		480582035	MANUFACTURE(66343-021)

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