EMVITA 21- lachesis muta venom, matricaria recutita, magnesium carbonate, arsenic trioxide, and sus scrofa pituitary gland liquid

Emvita 21 by

Drug Labeling and Warnings

Emvita 21 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: Physical overstrain

Ingredients

Lachesis mutus 800 C
Chamomilla 18 LM
Magnesia carbonica 21 x
Arsenicum alb. 21 x
Hypophysis 21 x
Alcohol 45 % 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 21

Homeopathic Combination
Medicine Indications:
Physical overstrain

RUBIMED®

1.7 Fl.oz. (50ml)

INGREDIENTS AND APPEARANCE

EMVITA 21 
lachesis muta venom, matricaria recutita, magnesium carbonate, arsenic trioxide, and sus scrofa pituitary gland liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-033
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	800 [hp_C]  in 1 mL
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	18 [hp_M]  in 1 mL
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D, MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM CARBONATE	21 [hp_X]  in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	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)	0.45 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-033-50	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(66343-033)

Establishment
Name	Address	ID/FEI	Business Operations
Omida AG		483268348	MANUFACTURE(66343-033)