NDC 0268-8029 Hickory Pecan Mix
Carya Illinoinensis Pollen,Carya Ovata Pollen Injection, Solution Subcutaneous - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0268 - Alk-abello, Inc.
- 0268-8029 - Hickory Pecan Mix
Product Packages
NDC Code 0268-8029-50
Package Description: 53 mL in 1 VIAL
Product Details
What is NDC 0268-8029?
What are the uses for Hickory Pecan Mix?
What are Hickory Pecan Mix Active Ingredients?
Which are Hickory Pecan Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- GIBBERELLA ZEAE (UNII: T9GHE8H4RX)
- GIBBERELLA ZEAE (UNII: T9GHE8H4RX) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- ASPERGILLUS REPENS (UNII: SQ89E6LOME)
- ASPERGILLUS REPENS (UNII: SQ89E6LOME) (Active Moiety)
- ASPERGILLUS FLAVUS VAR. ORYZAE (UNII: Q6Z8UK5R3G)
- ASPERGILLUS FLAVUS VAR. ORYZAE (UNII: Q6Z8UK5R3G) (Active Moiety)
- ASPERGILLUS TERREUS (UNII: QBN8K7055X)
- ASPERGILLUS TERREUS (UNII: QBN8K7055X) (Active Moiety)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (Active Moiety)
- PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M)
- PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- ANSER ANSER FEATHER (UNII: 15XI414745) (Active Moiety)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (Active Moiety)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
- BETULA LENTA WHOLE (UNII: 41A3V2257T)
- BETULA LENTA WHOLE (UNII: 41A3V2257T) (Active Moiety)
- ACER SACCHARINUM POLLEN (UNII: 95447163DG)
- ACER SACCHARINUM POLLEN (UNII: 95447163DG) (Active Moiety)
- CARYA OVATA POLLEN (UNII: 54UN9R2798)
- CARYA OVATA POLLEN (UNII: 54UN9R2798) (Active Moiety)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (Active Moiety)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (Active Moiety)
- PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK)
- PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (Active Moiety)
- ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I)
- ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I) (Active Moiety)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (Active Moiety)
Which are Hickory Pecan Mix 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Hickory Pecan Mix?
- RxCUI: 1922788 - giant ragweed pollen extract 100 UNT/ML / short ragweed pollen extract 100 UNT/ML Injectable Solution
- RxCUI: 1922788 - Ambrosia artemisiifolia pollen extract 100 PNU/ML / Ambrosia trifida pollen extract 100 PNU/ML Injectable Solution
- RxCUI: 1922788 - Ambrosia artemisiifolia pollen extract 100 UNT/ML / Ambrosia trifida pollen extract 100 UNT/ML Injectable Solution
- RxCUI: 1922791 - giant ragweed pollen extract 40000 UNT/ML / short ragweed pollen extract 40000 UNT/ML Injectable Solution
- RxCUI: 1922791 - Ambrosia artemisiifolia pollen extract 40000 PNU/ML / Ambrosia trifida pollen extract 40000 PNU/ML Injectable Solution
Which are the Pharmacologic Classes for Hickory Pecan Mix?
* 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.
[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".