NDC 43406-0115 Contact Allergy Antigen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43406-0115?
What are the uses for Contact Allergy Antigen?
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.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".