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

​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.

​Uses: ​(†) Homeopathic remedy for hectic.

​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 is 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 66343-054-50

RUBIMED

Emvita 5

1.7 fl oz Bottle Label

​ ​Homeopathic Medicine For

Hectic

1.7 fl oz. 50 mL    20% Ethanol

Homeopathic Medicine For

Hectic

EMVITA 5 
bufo rana, glandula suprarenalis, pulsatilla, cuprum metallicum, phosphorus, zincum metallicum liquid
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:66343-054
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q) BUFO BUFO CUTANEOUS GLAND800 [hp_C]  in 50 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND21 [hp_X]  in 50 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS16 [hp_M]  in 50 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER18 [hp_M]  in 50 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS21 [hp_X]  in 50 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC21 [hp_X]  in 50 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66343-054-5050 mL in 1 BOTTLE; Type 0: Not a Combination Product06/03/201912/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/03/201912/01/2021
Labeler - RUBIMED AG (480582035)

Revised: 1/2022
Document Id: b2cb0070-ce80-4274-a0f5-58421746d7f3
Set id: 1c59610f-91ca-450e-a0ec-caaad458b44c
Version: 3
Effective Time: 20220104
 
RUBIMED AG