EMVITA 16- aconitum napellus, ambra grisea, eschscholtzia, thymus gland, secale, zinc met liquid

Emvita 16 by

Drug Labeling and Warnings

Emvita 16 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: ​16.7% of each

Aconitum napellus 800C

Ambra grisea 18LM

Eschscholtzia 16LM           Secale 21X

Thymus gland 21X             Zinc Met 21X

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

INDICATIONS & USAGE

​Uses: ​(†) Homeopathic remedy for

feelings of panic.

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 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.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

www.privianaturals.com

1 (888) 526-9695 Product of USA.

PRINCIPAL DISPLAY PANEL

​NDC: 66343-065-50

RUBIMED

Emvita 16

​Homeopathic Medicine For

​Feelings Of Panic

​1.7 fl oz. 50 mL   20% Ethanol

​Homeopathic Medicine For

Feelings Of Panic

INGREDIENTS AND APPEARANCE

EMVITA 16 
aconitum napellus, ambra grisea, eschscholtzia, thymus gland, secale, zinc met liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 66343-065
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	800 [hp_C]  in 50 mL
AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C)	AMBERGRIS	18 [hp_M]  in 50 mL
ESCHSCHOLZIA CALIFORNICA (UNII: 9315HN272X) (ESCHSCHOLZIA CALIFORNICA - UNII:9315HN272X)	ESCHSCHOLZIA CALIFORNICA	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
CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (CLAVICEPS PURPUREA SCLEROTIUM - UNII:01G9XEA93N)	CLAVICEPS PURPUREA SCLEROTIUM	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: 66343-065-50	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)