EMVITA 7- anacard occ, lachesis mutus, phosphorus, glandula sup, lycopodium liquid
RUBIMED AG

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Emvita 7

Drug Facts

Active Ingredients: (HPUS*) 20% of each

Anacard occ 18LM Glandula sup 21X

Lachesis mutus 800C Lycopodium 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.

Uses: (†) Homeopathic remedy for show

of strength.

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.

Directions: (adults & children 6 years & older)

Take 5 drops 3 - 6 times daily, or as

recommended by your health care

professional.

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 ingredients: Ethanol 20% USP,

Purified Water.

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.

NDC 66343-056-50

RUBIMED

Emvita 7

1.7 fl oz. Bottle Label

Homeopathic Medicine For

Show of Strength

1.7 fl oz. 50 mL 20% Ethanol

Homeopathic Medicine For

Show of Strength

EMVITA 7
anacard occ, lachesis mutus, phosphorus, glandula sup, lycopodium liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:66343-056
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E)	ANACARDIUM OCCIDENTALE FRUIT	18 [hp_M] in 50 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	800 [hp_C] in 50 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	21 [hp_X] 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
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	16 [hp_M] in 50 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66343-056-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2019

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

Labeler - RUBIMED AG (480582035)

Revised: 1/2021

Document Id: b96efd18-f3fb-1ddb-e053-2a95a90a3e71

Set id: c0852bd9-f84c-4ff6-a491-af49f9a8da4b

Version: 2

Effective Time: 20210121

RUBIMED AG