EMVITA 5- bufo rana, glandula suprarenalis, pulsatilla, cuprum metallicum, phosphorus, zincum metallicum liquid

Emvita 5 by

Drug Labeling and Warnings

Emvita 5 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 Ingredents: ​(HPUS*) 16.7% of each

Bufo rana 800C      Cuprum metallicum 18LM

Glandula suprarenalis 21X     Phosphorus 21X

Pulsatilla 16LM             Zincum metallicum 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 hectic.

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 is 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: 66343-054-50

RUBIMED

Emvita 5

​​Homeopathic Medicine For

Hectic

1.7 fl oz. 50 mL    20% Ethanol

Homeopathic Medicine For

Hectic

INGREDIENTS AND APPEARANCE

EMVITA 5 
bufo rana, glandula suprarenalis, pulsatilla, cuprum metallicum, phosphorus, zincum metallicum liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 66343-054
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q)	BUFO BUFO CUTANEOUS GLAND	800 [hp_C]  in 50 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	21 [hp_X]  in 50 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	16 [hp_M]  in 50 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	18 [hp_M]  in 50 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	21 [hp_X]  in 50 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	21 [hp_X]  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: 66343-054-50	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)