1. Labeler Index
  2. Nelco Laboratories, Inc.
  3. NDC Product Code: 36987-1035 Goose Feathers

NDC 36987-1035 Goose Feathers

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 36987-1035?
    4. Goose Feathers 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.
NDC Product Code:
36987-1035
Proprietary Name:
Goose Feathers
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nelco Laboratories, Inc.
Labeler Code:
36987
Product Label ID:
001dcaf3-5838-4fb0-a4b8-d65ae2eb009e
Start Marketing Date: [9]
08-29-1972
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 36987-1035-1

Package Description: 5 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-1035-2

Package Description: 10 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-1035-3

Package Description: 30 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-1035-4

Package Description: 50 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 36987-1035?

The NDC code 36987-1035 is assigned by the FDA to the product Goose Feathers which is product labeled by Nelco Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 36987-1035-1 5 ml in 1 vial, multi-dose , 36987-1035-2 10 ml in 1 vial, multi-dose , 36987-1035-3 30 ml in 1 vial, multi-dose , 36987-1035-4 50 ml in 1 vial, multi-dose . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Goose Feathers?

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 Goose Feathers UNII Codes?

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

Which are Goose Feathers 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:

What is the NDC to RxNorm Crosswalk for Goose Feathers?

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: 889656 - hog skin extract 20000 UNT/mL Injectable Solution
  • RxCUI: 889656 - hog skin extract 20000 UNT/ML Injectable Solution
  • RxCUI: 889656 - Sus scrofa skin extract 20,000 UNT/ML Injectable Solution
  • RxCUI: 894778 - duck feather extract 20,000 UNT/mL Injectable Solution
  • RxCUI: 894778 - duck feather extract 20000 UNT/ML Injectable Solution

* Please review the disclaimer below.

Product Footnotes

[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".