NDC 62795-9489 Zeel
Alpha Lipoic Acid,Arnica Montana Whole, Sus Scrofa Cartilage,Coenzyme A, Solanum Dulcamara - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62795 - Medinatura Inc
- 62795-9489 - Zeel
Product Packages
NDC Code 62795-9489-8
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Details
What is NDC 62795-9489?
What are the uses for Zeel?
What are Zeel Active Ingredients?
- ALPHA LIPOIC ACID 6 [hp_X]/g - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
- ARNICA MONTANA WHOLE 2 [hp_X]/g
- COENZYME A 6 [hp_X]/g
- CORIANDER 8 [hp_X]/g
- NADIDE 6 [hp_X]/g
- SANGUINARIA CANADENSIS ROOT 2 [hp_X]/g
- SILICON DIOXIDE 6 [hp_X]/g - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SODIUM DIETHYL OXALACETATE 6 [hp_X]/g
- SOLANUM DULCAMARA TOP 2 [hp_X]/g
- SULFUR 6 [hp_X]/g - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- SUS SCROFA CARTILAGE 2 [hp_X]/g
- SUS SCROFA EMBRYO 2 [hp_X]/g
- SUS SCROFA PLACENTA 2 [hp_X]/g
- SUS SCROFA UMBILICAL CORD 2 [hp_X]/g
- TOXICODENDRON PUBESCENS LEAF 2 [hp_X]/g
Which are Zeel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- COENZYME A (UNII: SAA04E81UX)
- COENZYME A (UNII: SAA04E81UX) (Active Moiety)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO)
- SUS SCROFA EMBRYO (UNII: 9928MC12VO) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8)
- SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- CORIANDER (UNII: 1OV56052IK)
- CORIANDER (UNII: 1OV56052IK) (Active Moiety)
Which are Zeel 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALCOHOL (UNII: 3K9958V90M)
- PARAFFIN (UNII: I9O0E3H2ZE)
- WHITE PETROLATUM (UNII: B6E5W8RQJ4)
* Please review the disclaimer below.
[1] 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.
[2] 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.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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] 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".