NDC 63083-1026 Eastern Trees 1026
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-1026?
What are the uses for Eastern Trees 1026?
Which are Eastern Trees 1026 UNII Codes?
The UNII codes for the active ingredients in this product are:
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557)
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557) (Active Moiety)
- MILLETTIA PINNATA WHOLE (UNII: 11R319D14O)
- MILLETTIA PINNATA WHOLE (UNII: 11R319D14O) (Active Moiety)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976) (Active Moiety)
- ELM (UNII: 63POE2M46Y)
- ELM (UNII: 63POE2M46Y) (Active Moiety)
- CARYA LACINIOSA BARK (UNII: 98Q86P6WFR)
- CARYA LACINIOSA BARK (UNII: 98Q86P6WFR) (Active Moiety)
- ACER PENSYLVANICUM WHOLE (UNII: 01B3X858LI)
- ACER PENSYLVANICUM WHOLE (UNII: 01B3X858LI) (Active Moiety)
- QUERCUS KELLOGGII POLLEN (UNII: 02RVY6X9EC)
- QUERCUS KELLOGGII POLLEN (UNII: 02RVY6X9EC) (Active Moiety)
- LIRIODENDRON TULIPIFERA WHOLE (UNII: 0601Z4Z0LU)
- LIRIODENDRON TULIPIFERA WHOLE (UNII: 0601Z4Z0LU) (Active Moiety)
- LIQUIDAMBAR STYRACIFLUA RESIN (UNII: P41GWD11CX)
- LIQUIDAMBAR STYRACIFLUA RESIN (UNII: P41GWD11CX) (Active Moiety)
- SYMPHORICARPOS ALBUS FRUIT (UNII: 873JZU3ASZ)
- SYMPHORICARPOS ALBUS FRUIT (UNII: 873JZU3ASZ) (Active Moiety)
Which are Eastern Trees 1026 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)
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[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".