EMVITA 5- bufo rana, cuprum metallicum, glandula suprarenalis, phosphorus, pulsatilla, 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 Ingredients: (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 general well being: nervousness.

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: 66343-092-60

RUBIMED

Emvita 5

Homeopathic Medicine For

General Well-being: 

Nervousness

2.0 fl oz. 59mL 20% Ethanol

Homeopathic Medicine For

General Well-being:

Nervousness

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-092
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 60 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	18 [hp_M]  in 60 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	21 [hp_X]  in 60 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	21 [hp_X]  in 60 mL
PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	PULSATILLA VULGARIS WHOLE	16 [hp_M]  in 60 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	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: 66343-092-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/21/2022

Labeler - RUBIMED AG (480582035)