EMVITA 22- ambra grisea, anacard occ, chamomilla, crotalus horridus, hypophysis, iodium, phosphorus 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 components 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 general well being: feeling restless.

WARNINGS

Warnings:

Stop use if symptoms persist or worsen.

If you are pregnant or breastfeeding,consult a healthcare professional prior to use. 

Keep out of reach of children. 

DOSAGE & ADMINISTRATION

Directions: (adults & children 6 years & older)

Take 12 drops 2 times daily, or as recommended by your health care professional. 

OTHER SAFETY INFORMATION

Other information: Store at 20 - 25°C

(68 - 77°F.) 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.

9169 W State St #196

Garden City, ID 83714

www.privianaturals.com

Info@privianaturals.com Product of USA.

PRINCIPAL DISPLAY PANEL

NDC: 66343-109-60

RUBIMED

Emvita 22

Homeopathic Medicine For

General Well-being: 

Feeling Restless

2.0 fl oz. 59mL 20% Ethanol

Homeopathic Medicine For

General Well-being:

Feeling Restless

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-109
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 60 mL
ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E)	ANACARDIUM OCCIDENTALE FRUIT	18 [hp_M]  in 60 mL
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ)	MATRICARIA CHAMOMILLA WHOLE	800 [hp_C]  in 60 mL
CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ956)	CROTALUS HORRIDUS HORRIDUS VENOM	21 [hp_X]  in 60 mL
SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT)	SUS SCROFA PITUITARY GLAND	21 [hp_X]  in 60 mL
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	16 [hp_M]  in 60 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	21 [hp_X]  in 60 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: 66343-109-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/23/2022

Labeler - RUBIMED AG (480582035)