EMVITA 24- crotalus horridus horridus venom, phosphorus, matricaria recutita, strychnos ignatii seed, and sus scrofa pituitary gland liquid

Emvita 24 by

Drug Labeling and Warnings

Emvita 24 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: Feeling of discomfort

Ingredients

Crotalus horridus 800 C
Phosphorus 16 LM
Chamomilla 18 LM
Ignatia amara 21 x
Hypophysis 21 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 24

Homeopathic Combination
Medicine Indications:
Feeling of discomfort

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 24 
crotalus horridus horridus venom, phosphorus, matricaria recutita, strychnos ignatii seed, and sus scrofa pituitary gland liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-036
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ956)	CROTALUS HORRIDUS HORRIDUS VENOM	800 [hp_C]  in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	16 [hp_M]  in 1 mL
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	18 [hp_M]  in 1 mL
STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K)	STRYCHNOS IGNATII SEED	21 [hp_X]  in 1 mL
SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T)	SUS SCROFA PITUITARY GLAND	21 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)	0.38 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-036-50	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(66343-036)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-036)