Emvita 13
- Manufacturer
- RUBIMED AG
- Effective date
- 2021-01-21
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:55:41
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
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.
INDICATIONS & USAGE SECTION
Uses: (†) Homeopathic remedy for
withdrawn.
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
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 if 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 66343-062-50
RUBIMED
Emvita 13
Homeopathic Medicine For
Withdrawn
1.7 fl oz. 50 mL 20% Ethanol
OTC - PURPOSE SECTION
Homeopathic Medicine For
Withdrawn
Products#
Every source-derived product name is available through these pages.
- Emvita 13
- Anacard occ, Calc carb, Thymus gland, Bothrops, Graphites
- ALCOHOL
- WATER
- ANACARDIUM OCCIDENTALE FRUIT
- OYSTER SHELL CALCIUM CARBONATE, CRUDE
- SUS SCROFA THYMUS
- BOTHROPS ATROX VENOM
- GRAPHITE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 66343-062 | 66343-062-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| ANACARDIUM OCCIDENTALE FRUIT | 4A10JR4E7E | ACTIB |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 2E32821G6I | ACTIB |
| SUS SCROFA THYMUS | 7B69B0BD62 | ACTIB |
| BOTHROPS ATROX VENOM | K0Q6REZ9JC | ACTIB |
| GRAPHITE | 4QQN74LH4O | 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 |
|---|---|---|---|---|---|---|
| 6de286ff-d813-4f7e-853f-82df5e5fda35 | bf65f4f6-57f0-4b1d-9296-ed430259adf1 | 2022-01-05 | Warnings | bf65f4f6-57f0-4b1d-9296-ed430259adf1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
