EMVITA 13- anacard occ, calc carb, thymus gland, bothrops, graphites 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 13

Drug Facts

Active Ingredients: 20% of each

Anacard occ 21X Bothrops 800C

Calc carb 16LM Graphites 18LM

Thymus gland 21X

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

Uses: (†) Homeopathic remedy for

withdrawn.

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.

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 66343-062-50

RUBIMED

Emvita 13

1.7 fl oz. Bottle Label

Homeopathic Medicine For

Withdrawn

1.7 fl oz. 50 mL 20% Ethanol

Homeopathic Medicine For

Withdrawn

EMVITA 13
anacard occ, calc carb, thymus gland, bothrops, graphites liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:66343-062
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	21 [hp_X] in 50 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	16 [hp_M] in 50 mL
SUS SCROFA THYMUS (UNII: 7B69B0BD62) (SUS SCROFA THYMUS - UNII:7B69B0BD62)	SUS SCROFA THYMUS	21 [hp_X] in 50 mL
BOTHROPS ATROX VENOM (UNII: K0Q6REZ9JC) (BOTHROPS ATROX VENOM - UNII:K0Q6REZ9JC)	BOTHROPS ATROX VENOM	800 [hp_C] in 50 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	18 [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:66343-062-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2019	12/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		06/03/2019	12/01/2021

Labeler - RUBIMED AG (480582035)

Revised: 1/2022

Document Id: 6de286ff-d813-4f7e-853f-82df5e5fda35

Set id: bf65f4f6-57f0-4b1d-9296-ed430259adf1

Version: 3

Effective Time: 20220105

RUBIMED AG