Emvita 5
- Manufacturer
- RUBIMED AG
- Effective date
- 2021-01-21
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:55:30
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
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.
INDICATIONS & USAGE SECTION
Uses: (†) Homeopathic remedy for hectic.
WARNINGS SECTION
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.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
DOSAGE & ADMINISTRATION SECTION
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 is safety seal of the
bottle is broken.
INACTIVE INGREDIENT SECTION
Inactive ingredients: Ethanol 20% USP,
Purified Water.
OTC - QUESTIONS SECTION
Manufactured by: OHM pharma, Inc., USA.
Distributed by: Privia Naturals, LLC.
197 Woodland Pkwy Suite 104 #813
San Marcos, CA 92069
1 (888) 526-9695 Product of USA.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 66343-054-50
RUBIMED
Emvita 5
Homeopathic Medicine For
Hectic
1.7 fl oz. 50 mL 20% Ethanol
OTC - PURPOSE SECTION
Homeopathic Medicine For
Hectic
Products#
Every source-derived product name is available through these pages.
- Emvita 5
- Bufo rana, Glandula suprarenalis, Pulsatilla, Cuprum metallicum, Phosphorus, Zincum metallicum
- ALCOHOL
- WATER
- BUFO BUFO CUTANEOUS GLAND
- SUS SCROFA ADRENAL GLAND
- PULSATILLA VULGARIS
- COPPER
- PHOSPHORUS
- ZINC
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 66343-054 | 66343-054-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| BUFO BUFO CUTANEOUS GLAND | Q59QU6N72Q | ACTIB |
| SUS SCROFA ADRENAL GLAND | 398IYQ16YV | ACTIB |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| COPPER | 789U1901C5 | ACTIB |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| ZINC | J41CSQ7QDS | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| b2cb0070-ce80-4274-a0f5-58421746d7f3 | 1c59610f-91ca-450e-a0ec-caaad458b44c | 2022-01-04 | Warnings | 1c59610f-91ca-450e-a0ec-caaad458b44c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
