NEUROVITA- melissa officinalis, sus scrofa cerebellum, ambergris, cinchona officinalis bark, cupric acetate, and phosphorus liquid

Neurovita by

Drug Labeling and Warnings

Neurovita by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG, Omida AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Homeopathic Combination Medicine Indications: For nervous tension

Ingredients

Melissa 4 x
Cerebellum suis 21 x
Ambra grisea 21 x
Cinchona 50 C
Cuprum acet. 200 C
Phosphorus 12 LM
Alcohol 46 % 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

Neurovita

Homeopathic Combination
Medicine Indications:
For nervous tension

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

NEUROVITA 
melissa officinalis, sus scrofa cerebellum, ambergris, cinchona officinalis bark, cupric acetate, and phosphorus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-003
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N)	MELISSA OFFICINALIS	4 [hp_X]  in 1 mL
SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (SUS SCROFA CEREBELLUM - UNII:49NGK53TPQ)	SUS SCROFA CEREBELLUM	21 [hp_X]  in 1 mL
AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C)	AMBERGRIS	21 [hp_X]  in 1 mL
CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB)	CINCHONA OFFICINALIS BARK	50 [hp_C]  in 1 mL
CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L)	CUPRIC ACETATE	200 [hp_C]  in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	12 [hp_M]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)	0.46 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-003-50	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(66343-003)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-003)