NDC 49288-0331 Oak Mixture
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49288-0331?
What are the uses for Oak Mixture?
Which are Oak Mixture UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALIX LUCIDA SSP. LASIANDRA POLLEN (UNII: 9P9T267QMR)
- SALIX LUCIDA SSP. LASIANDRA POLLEN (UNII: 9P9T267QMR) (Active Moiety)
- JUGLANS REGIA POLLEN (UNII: ARW43087I1)
- JUGLANS REGIA POLLEN (UNII: ARW43087I1) (Active Moiety)
- SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN)
- SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (Active Moiety)
- SALIX DISCOLOR POLLEN (UNII: ER172J09FM)
- SALIX DISCOLOR POLLEN (UNII: ER172J09FM) (Active Moiety)
- AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3)
- AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (Active Moiety)
- PINUS CONTORTA POLLEN (UNII: FB7IP650ET)
- PINUS CONTORTA POLLEN (UNII: FB7IP650ET) (Active Moiety)
- JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I)
- JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (Active Moiety)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
- FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX)
- FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX) (Active Moiety)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
- BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML)
- BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML) (Active Moiety)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52)
- MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (Active Moiety)
- MORUS ALBA POLLEN (UNII: 3I9T68187H)
- MORUS ALBA POLLEN (UNII: 3I9T68187H) (Active Moiety)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA ALBA POLLEN (UNII: G2A764T54B) (Active Moiety)
- CARYA CORDIFORMIS POLLEN (UNII: O99P60FU6G)
- CARYA CORDIFORMIS POLLEN (UNII: O99P60FU6G) (Active Moiety)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A)
- CARYA GLABRA POLLEN (UNII: KPO1Z9N98A) (Active Moiety)
- CARYA OVATA POLLEN (UNII: 54UN9R2798)
- CARYA OVATA POLLEN (UNII: 54UN9R2798) (Active Moiety)
- QUERCUS VELUTINA POLLEN (UNII: 294L626TT0)
- QUERCUS VELUTINA POLLEN (UNII: 294L626TT0) (Active Moiety)
- QUERCUS MACROCARPA POLLEN (UNII: 57BTU4547U)
- QUERCUS MACROCARPA POLLEN (UNII: 57BTU4547U) (Active Moiety)
- QUERCUS MUEHLENBERGII POLLEN (UNII: 434DQ2U4JX)
- QUERCUS MUEHLENBERGII POLLEN (UNII: 434DQ2U4JX) (Active Moiety)
- QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO)
- QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (Active Moiety)
- QUERCUS RUBRA POLLEN (UNII: SVW19ET93C)
- QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (Active Moiety)
- QUERCUS PALUSTRIS POLLEN (UNII: CU781COT7M)
- QUERCUS PALUSTRIS POLLEN (UNII: CU781COT7M) (Active Moiety)
- QUERCUS STELLATA POLLEN (UNII: W34X0P8636)
- QUERCUS STELLATA POLLEN (UNII: W34X0P8636) (Active Moiety)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (Active Moiety)
Which are Oak Mixture 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORATE (UNII: T95DR77GMR)
What is the NDC to RxNorm Crosswalk for Oak Mixture?
- RxCUI: 1013964 - bald cypress pollen extract 50 MG/ML Injectable Solution
- RxCUI: 1013964 - bald cypress pollen extract 0.05 GM/ML Injectable Solution
- RxCUI: 1013964 - Taxodium distichum pollen extract 0.05 GM/ML Injectable Solution
- RxCUI: 1013964 - Taxodium distichum pollen extract 50 MG/ML Injectable Solution
- RxCUI: 1014194 - cedar elm pollen extract 50 MG/ML Injectable Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[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".