NDC 43406-0714 Contact Allergy Antigen
Toxicodendron Diversilobum Leaf,Toxicodendron Pubescens Leaf,Toxicodendron Vernix Leafy - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43406 - Natural Creations, Inc.
- 43406-0714 - Contact Allergy Antigen
Product Packages
NDC Code 43406-0714-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43406-0714?
What are the uses for Contact Allergy Antigen?
What are Contact Allergy Antigen Active Ingredients?
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- GRAPHITE 12 [hp_X]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- SEMECARPUS ANACARDIUM FRUIT 12 [hp_X]/mL
- TOXICODENDRON DIVERSILOBUM LEAF 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
- TOXICODENDRON VERNIX LEAFY TWIG 30 [hp_X]/mL
- URTICA DIOICA 30 [hp_X]/mL - A plant species of the genus Urtica, family URTICACEAE. Roots have been used to treat PROSTATIC HYPERPLASIA. Leaves are edible after the stinging quality is eliminated by brief heating.
- URTICA URENS 12 [hp_X]/mL
- XEROPHYLLUM ASPHODELOIDES 15 [hp_X]/mL
Which are Contact Allergy Antigen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ)
- TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- TOXICODENDRON VERNIX LEAFY TWIG (UNII: Y3VW699H96)
- TOXICODENDRON VERNIX LEAFY TWIG (UNII: Y3VW699H96) (Active Moiety)
- URTICA DIOICA (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- SEMECARPUS ANACARDIUM FRUIT (UNII: 7399B063X9)
- SEMECARPUS ANACARDIUM FRUIT (UNII: 7399B063X9) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B)
- XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (Active Moiety)
Which are Contact Allergy Antigen 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".