NDC 66343-110 Emvita 23
Agaricus Muscarius, Cuprum Met, Hypophysis, Rhus Tox Liquid Oral

Product Information

What is NDC 66343-110?

The NDC code 66343-110 is assigned by the FDA to the product Emvita 23 which is a human over the counter drug product labeled by Rubimed Ag. The generic name of Emvita 23 is agaricus muscarius, cuprum met, hypophysis, rhus tox. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 66343-110-60 60 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code66343-110
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Emvita 23
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Agaricus Muscarius, Cuprum Met, Hypophysis, Rhus Tox
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Rubimed Ag
Labeler Code66343
Marketing Category What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
NDC Code Structure

What are the uses for Emvita 23?

Product Packages

NDC Code 66343-110-60

Package Description: 60 mL in 1 BOTTLE

Product Details

What are Emvita 23 Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Emvita 23 Active Ingredients UNII Codes

  • COPPER (UNII: 789U1901C5)
  • COPPER (UNII: 789U1901C5) (Active Moiety)

Emvita 23 Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Emvita 23 Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Otc - Active Ingredient

Drug Facts Active Ingredients: (HPUS*) 25% of each

Agaricus muscarius 21X
Cuprum met 800C
Hypophysis 21X
Rhus tox 18LM

*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

Uses: (†) Homeopathic remedy for general well being: tenseness.



Stop use if symptoms persist or worsen.

If you are pregnant or breastfeeding, consult a healthcare professional prior to use. 

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. 

Dosage & Administration

Directions: (adults & children 6 years & older)

Take 12 drops 2 times daily, or as recommended by your health care professional. 

Other Safety Information

Other information: Store at 20 - 25°C

(68 - 77°F.) 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.

Otc - Questions

Manufactured by: OHM pharma, Inc, USA.

Distributed by: Privia Naturals, LLC.

9169 W State St #196

Garden City, ID 83714


[email protected] Product of USA.

Package Label.Principal Display Panel

NDC 66343-110-60


Emvita 23

Homeopathic Medicine For

General Well-being: 


2.0 fl oz. 59mL 20% Ethanol

Otc - Purpose

Homeopathic Medicine For

General Well-being:


* Please review the disclaimer below.