NDC 22840-1356 Nettle
Urtica Dioica Solution Intradermal; Percutaneous; Subcutaneous - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 22840 - Greer Laboratories, Inc.
- 22840-1356 - Nettle
Product Packages
NDC Code 22840-1356-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 22840-1356-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 22840-1356?
What are the uses for Nettle?
What are Nettle Active Ingredients?
Which are Nettle UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
- CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
- AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
- XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
- AMBROSIA BIDENTATA POLLEN (UNII: M3S672G75O)
- AMBROSIA BIDENTATA POLLEN (UNII: M3S672G75O) (Active Moiety)
- SALSOLA KALI POLLEN (UNII: 2MH135KC6G)
- SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (Active Moiety)
- AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX)
- AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (Active Moiety)
- ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I)
- ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I) (Active Moiety)
- AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH)
- AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83)
- ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (Active Moiety)
- RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
- RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (Active Moiety)
- RUMEX CRISPUS POLLEN (UNII: V825XJG64G)
- RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (Active Moiety)
- ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI)
- ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI) (Active Moiety)
- AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L)
- AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (Active Moiety)
- AMARANTHUS HYBRIDUS POLLEN (UNII: EK7F0414PI)
- AMARANTHUS HYBRIDUS POLLEN (UNII: EK7F0414PI) (Active Moiety)
- AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y)
- AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (Active Moiety)
- CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J)
- CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (Active Moiety)
- ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O)
- ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O) (Active Moiety)
- AMBROSIA DUMOSA POLLEN (UNII: ZIO18VN6HJ)
- AMBROSIA DUMOSA POLLEN (UNII: ZIO18VN6HJ) (Active Moiety)
- BACCHARIS SAROTHROIDES WHOLE (UNII: C94X53K2GW)
- BACCHARIS SAROTHROIDES WHOLE (UNII: C94X53K2GW) (Active Moiety)
- BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW)
- BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW) (Active Moiety)
- ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H)
- ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H) (Active Moiety)
- AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP)
- AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP) (Active Moiety)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
- ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD)
- ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (Active Moiety)
- AMBROSIA CONFERTIFLORA POLLEN (UNII: 63TBJ590BL)
- AMBROSIA CONFERTIFLORA POLLEN (UNII: 63TBJ590BL) (Active Moiety)
- ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU)
- ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU) (Active Moiety)
- BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
- BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (Active Moiety)
- AMBROSIA SALSOLA POLLEN (UNII: 662J7FTA7T)
- AMBROSIA SALSOLA POLLEN (UNII: 662J7FTA7T) (Active Moiety)
- EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0)
- EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (Active Moiety)
- SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5)
- SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (Active Moiety)
- AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G)
- AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (Active Moiety)
- IVA ANNUA POLLEN (UNII: Y2U5S5PF22)
- IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- URTICA DIOICA POLLEN (UNII: DNB59M1NVU)
- URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (Active Moiety)
Which are Nettle 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 BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Nettle?
- RxCUI: 1006361 - Canada goldenrod pollen extract 100 MG/ML Injectable Solution
- RxCUI: 1006361 - Solidago canadensis pollen extract 0.1 GM/ML Injectable Solution
- RxCUI: 1006361 - Solidago canadensis pollen extract 100 MG/ML Injectable Solution
- RxCUI: 1006365 - Canada goldenrod pollen extract 20,000 UNT/mL Injectable Solution
- RxCUI: 1006365 - Canada goldenrod pollen extract 20000 UNT/ML Injectable Solution
Which are the Pharmacologic Classes for Nettle?
* 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".