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

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)

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)	0.45 mL in 1 mL

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

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