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

Simvita by

Drug Labeling and Warnings

Simvita by is a Homeopathic 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: For feeling restless

ACTIVE INGREDIENT

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)

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

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

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

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