SIMVITA- claviceps purpurea sclerotium, sus scrofa cerebellum, epinephrine, and tuberculin purified protein derivative 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.

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Simvita

Homeopathic Combination Medicine Indications: For feeling restless

Ingredients

Secale cornutum. 12 x
Cerebellum suis 21 X
Adrenalinum hydrocl 30 x
Tuberculinum 200 C
Alcohol 51 % v/v

TAMPER-EVIDENT

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

Direction

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

Simvita

Homeopathic Combination
Medicine Indications:
For feeling restless

RUBIMED®

1.7 Fl.oz. (50 ml)

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

SIMVITA
claviceps purpurea sclerotium, sus scrofa cerebellum, epinephrine, and tuberculin purified protein derivative liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66343-005
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Claviceps Purpurea Sclerotium (UNII: 01G9XEA93N) (Claviceps Purpurea Sclerotium - UNII:01G9XEA93N)	Claviceps Purpurea Sclerotium	12 [hp_X] in 1 mL
Sus Scrofa Cerebellum (UNII: 49NGK53TPQ) (Sus Scrofa Cerebellum - UNII:49NGK53TPQ)	Sus Scrofa Cerebellum	21 [hp_X] in 1 mL
Epinephrine (UNII: YKH834O4BH) (Epinephrine - UNII:YKH834O4BH)	Epinephrine	30 [hp_X] in 1 mL
Tuberculin Purified Protein Derivative (UNII: I7L8FKN87J) (Tuberculin Purified Protein Derivative - UNII:I7L8FKN87J)	Tuberculin Purified Protein Derivative	200 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Alcohol (UNII: 3K9958V90M)	0.51 mL in 1 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66343-005-50	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(66343-005)

Name	Address	ID/FEI	Business Operations
Establishment
Omida AG		483268348	MANUFACTURE(66343-005)