EMVITA 19- calcarea carbonica, mag carb, hypophysis, zinc met liquid

Emvita 19 by

Drug Labeling and Warnings

Emvita 19 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*) 25% of each

Calcarea carbonica 21X      Hypophysis 21X

Mag carb 800C                   Zinc met 18LM

*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

feelings of faintheartedness.

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 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: 66343-068-50

RUBIMED

Emvita 19

​​Homeopathic Medicine For

Feelings Of Faintheartedness

1.7 fl oz. 50mL    20% Ethanol

Homeopathic Medicine For

Feelings Of Faintheartedness

INGREDIENTS AND APPEARANCE

EMVITA 19 
calcarea carbonica, mag carb, hypophysis, zinc met liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 66343-068
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	21 [hp_X]  in 50 mL
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D)	MAGNESIUM CARBONATE	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
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	18 [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: 66343-068-50	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)