NDC 43742-2043 Ver
Artemisia Vulgaris, Ascaris Lumbricoides, Brugia Malayi, Calcarea Carbonica, Cina, Cr...

Product Information

NDC Product Code43742-2043
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.		Ver
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.		Artemisia Vulgaris, Ascaris Lumbricoides, Brugia Malayi, Calcarea Carbonica, Cina, Cryptosporidium Parvum, Enterobius Vermicularis, Filix Mas, Giardia Lamblia, Graphites, Iodium, Mercurius Corrosivus, Quassia (amara), Sabadilla, Silicea, Spigelia Anthelmia, Taenia Saginata, Taenia Solium, Teucrium Marum, Thymus Serpyllum, Trichinella Spiralis, Trichomonas Vaginalis
Substance Name What is the Substance Name?
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.		Artemisia Cina Pre-flowering Top; Artemisia Vulgaris Root; Ascaris Lumbricoides; Brugia Malayi; Cryptosporidium Parvum; Dryopteris Filix-mas Root; Enterobius Vermicularis; Giardia Lamblia; Graphite; Iodine; Mercuric Chloride; Oyster Shell Calcium Carbonate, Crude; Quassia Amara Wood; Schoenocaulon Officinale Seed; Silicon Dioxide; Spigelia Anthelmia Whole; Taenia Saginata; Taenia Solium; Teucrium Marum Whole; Thymus Serpyllum Whole; Trichinella Spiralis; Trichomonas Vaginalis
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
NDC Directory StatusACTIVE PRODUCT and included in NDC Directory
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.		Deseret Biologicals, Inc.
Labeler Code43742
SPL SET ID:b47bdd57-14cd-46e9-a34e-0d8a7c21bda2
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.		UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
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.		03-10-2023
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.		12-31-2024
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". 		N
NDC Code Structure

Product Packages

NDC Code 43742-2043-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 43742-2043?

The NDC code 43742-2043 is assigned by the FDA to the product Ver which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Ver is artemisia vulgaris, ascaris lumbricoides, brugia malayi, calcarea carbonica, cina, cryptosporidium parvum, enterobius vermicularis, filix mas, giardia lamblia, graphites, iodium, mercurius corrosivus, quassia (amara), sabadilla, silicea, spigelia anthelmia, taenia saginata, taenia solium, teucrium marum, thymus serpyllum, trichinella spiralis, trichomonas vaginalis. 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 43742-2043-1 60 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Ver?

For temporary relief of symptoms related to parasite infestation including occasional diarrhea, digestive problems, flatulence, occasional constipation, and spasms.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

What are Ver 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.

Which are Ver UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Ver 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. The UNII codes for the inactive ingredients in this product are:

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Product Label

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