Wingscale
NDC 36987-3440

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 36987-3440?
  4. Wingscale Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Wingscale is a BLA-approved product labeled by Nelco Laboratories, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 36987-3440 and 4 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
36987-3440
Proprietary Name:
Wingscale
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Nelco Laboratories, Inc.
Labeler Code:
36987
Product Label ID:
7f312e04-f414-4f1e-bce2-ea43fe3d93f9
FDA Application Number: [6]
BLA102192
Marketing Category: [8]
BLA - A product marketed under an approved Biologic License Application.

Marketing Timeline

Start Marketing Date: [9]
08-29-1972
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 36987-3440?

The NDC code 36987-3440 is assigned by the FDA to the product Wingscale. This pharmaceutical product is labeled by Nelco Laboratories, Inc. and is currently categorized as listed product. In terms of distribution, this product is available in 4 different package configurations. The associated package NDC(s) include: 36987-3440-1, 36987-3440-2, 36987-3440-3, 36987-3440-4. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY)
  • TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY) (Active Moiety)
  • ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU)
  • ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU) (Active Moiety)
  • BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW)
  • BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW) (Active Moiety)
  • HYMENOCLEA SALSOLA POLLEN (UNII: 662J7FTA7T)
  • HYMENOCLEA SALSOLA POLLEN (UNII: 662J7FTA7T) (Active Moiety)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
  • RUMEX CRISPUS POLLEN (UNII: V825XJG64G)
  • RUMEX CRISPUS (UNII: S9T422Q956) (Active Moiety)
  • EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0)
  • EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (Active Moiety)
  • KOCHIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
  • KOCHIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (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)
  • ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI)
  • ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI) (Active Moiety)
  • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
  • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
  • ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I)
  • ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I) (Active Moiety)
  • IVA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J)
  • IVA ANGUSTIFOLIA POLLEN (UNII: UBW6O1H50I) (Active Moiety)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22) (Active Moiety)
  • CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H)
  • CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (Active Moiety)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
  • ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H)
  • ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H) (Active Moiety)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (Active Moiety)
  • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH)
  • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (Active Moiety)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N) (Active Moiety)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
  • IVA AXILLARIS POLLEN (UNII: 13KFG30UBR)
  • IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (Active Moiety)
  • AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP)
  • AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP) (Active Moiety)
  • CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X)
  • CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (Active Moiety)
  • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3)
  • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (Active Moiety)
  • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y)
  • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (Active Moiety)
  • SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X)
  • SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X) (Active Moiety)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (Active Moiety)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (Active Moiety)
  • ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD)
  • ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (Active Moiety)
  • ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O)
  • ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O) (Active Moiety)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (Active Moiety)
  • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L)
  • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (Active Moiety)
  • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83)
  • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (Active Moiety)

Which are the Inactive Ingredients associated 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:

What is the NDC to RxNorm Crosswalk for this product?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1006357 - Russian thistle pollen extract 20000 UNT/ML Injectable Solution
  • RxCUI: 1006357 - Salsola kali pollen extract 20,000 UNT/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
  • RxCUI: 1006365 - Solidago canadensis pollen extract 20,000 UNT/ML Injectable Solution

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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".