NDC 36987-2614 Arizona Cypress
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36987 - Nelco Laboratories, Inc.
- 36987-2614 - Arizona Cypress
Product Packages
NDC Code 36987-2614-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2614-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2614-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2614-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-2614?
What are the uses for Arizona Cypress?
Which are Arizona Cypress UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACACIA BAILEYANA POLLEN (UNII: 59WAV8G5X5)
- ACACIA BAILEYANA POLLEN (UNII: 59WAV8G5X5) (Active Moiety)
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H)
- ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (Active Moiety)
- ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5)
- ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (Active Moiety)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM)
- ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (Active Moiety)
- FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD)
- FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (Active Moiety)
- FRAXINUS LATIFOLIA POLLEN (UNII: 1FH355G8HF)
- FRAXINUS LATIFOLIA POLLEN (UNII: 1FH355G8HF) (Active Moiety)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
- POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA)
- POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (Active Moiety)
- MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89)
- MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (Active Moiety)
- FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4)
- FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (Active Moiety)
- CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N)
- CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (Active Moiety)
- BETULA NIGRA POLLEN (UNII: 93963RFO1P)
- BETULA NIGRA POLLEN (UNII: 93963RFO1P) (Active Moiety)
- BETULA LENTA POLLEN (UNII: JQ5HI5004M)
- BETULA LENTA POLLEN (UNII: JQ5HI5004M) (Active Moiety)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (Active Moiety)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (Active Moiety)
- JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y)
- JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (Active Moiety)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G)
- JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (Active Moiety)
- TAMARIX GALLICA POLLEN (UNII: 43IR7KR479)
- TAMARIX GALLICA POLLEN (UNII: 43IR7KR479) (Active Moiety)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (Active Moiety)
- POPULUS FREMONTII POLLEN (UNII: 426RHB4302)
- POPULUS FREMONTII POLLEN (UNII: 426RHB4302) (Active Moiety)
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441)
- POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (Active Moiety)
- CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF)
- CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (Active Moiety)
Which are Arizona Cypress 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)
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Arizona Cypress?
- RxCUI: 1006474 - mango blossom pollen extract 10000 UNT/ML Injectable Solution
- RxCUI: 1006474 - Mangifera indica pollen extract 10,000 UNT/ML Injectable Solution
- RxCUI: 1006480 - black oak pollen extract 10000 UNT/ML Injectable Solution
- RxCUI: 1006480 - Quercus velutina pollen extract 10,000 UNT/ML Injectable Solution
- RxCUI: 1013878 - eastern white pine pollen extract 10,000 UNT/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.
[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".