EMVITA 22- ambra grisea, chamomilla, hypophysis, phosphorus, anacard occ, crotalus horridus, iodum liquid

Emvita 22 by

Drug Labeling and Warnings

Emvita 22 by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

​Drug Facts

​Active Ingredients: ​(HPUS*) 14.3% of each

Ambra grisea 21X       Anacard occ 18LM

Chamomilla 800C         Crotalus horridus 21X

Hypophysis 21X          Iodium 16LM

Phosphorus 21X

*The letters "HPUS" indicate that the

component in this product are officially

monographed in the Homeopathic

Pharmacopoeia of the United States.

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

INDICATIONS & USAGE

​Uses: ​(†) Homeopathic remedy for

feelings of restlessness.

WARNINGS

​Warnings:

Stop use if symptoms persist or worsen.

​If you are pregnant or breastfeeding,

​consult a health care professional prior to use.

​Keep out of reach of children.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

​Directions: ​(adults & children 6 years & older)

Take 5 drops 3 - 6 times daily, or as

recommended by your health care

professional.

OTHER SAFETY INFORMATION

​Other information: ​Store at 20 - 25ºC

(68 - 77ºF). Do not use if box has been

tampered with, or if the safety seal of the

bottle is broken.

INACTIVE INGREDIENT

​Inactive ingredients: ​Ethanol 20% USP,

Purified Water.

QUESTIONS

Manufactured by: OHM pharma, Inc., USA.

Distributed by: Privia Naturals, LLC.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

www.privianaturals.com

1 (888) 526-9695 Product of USA.

PRINCIPAL DISPLAY PANEL

​NDC: 66343-071-50

RUBIMED

Emvita 22

​Homeopathic Medicine For

​Feelings Of Restlessness

​1.7 fl oz. 50 mL    20% Ethanol

​Homeopathic Medicine For

Feelings Of Restlessness

INGREDIENTS AND APPEARANCE

EMVITA 22 
ambra grisea, chamomilla, hypophysis, phosphorus, anacard occ, crotalus horridus, iodum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-071
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C)	AMBERGRIS	21 [hp_X]  in 50 mL
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ)	MATRICARIA CHAMOMILLA	800 [hp_C]  in 50 mL
SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT)	SUS SCROFA PITUITARY GLAND	21 [hp_X]  in 50 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	21 [hp_X]  in 50 mL
ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E)	ANACARDIUM OCCIDENTALE FRUIT	18 [hp_X]  in 50 mL
CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ956)	CROTALUS HORRIDUS HORRIDUS VENOM	21 [hp_X]  in 50 mL
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	16 [hp_M]  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-071-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/03/2019

Labeler - RUBIMED AG (480582035)