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  4. NDC Product Code: 22840-0301 Short And Giant Ragweed Pollen Mix

NDC 22840-0301 Short And Giant Ragweed Pollen Mix

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 22840-0301?
  4. Short And Giant Ragweed Pollen Mix 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:
22840-0301
Proprietary Name:
Short And Giant Ragweed Pollen Mix
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Greer Laboratories, Inc.
Labeler Code:
22840
Product Label ID:
60b52a1c-8f5e-2302-e053-2991aa0a601a
Start Marketing Date: [9]
09-15-1981
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 22840-0301?

The NDC code 22840-0301 is assigned by the FDA to the product Short And Giant Ragweed Pollen Mix which is product labeled by Greer Laboratories, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 22840-0301-2 10 ml in 1 vial, multi-dose , 22840-0301-4 50 ml in 1 vial, multi-dose , 22840-0301-5 5 ml in 1 bottle, dropper . 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 Short And Giant Ragweed Pollen Mix?

INDICATIONSHyposensitization is indicated when careful testing and patient history can pinpoint allergens responsible for allergic symptoms, and when it is not possible or practical to avoid these allergens. Allergenic extracts are administered to reduce symptoms of allergy of a seasonal or perennial nature.

Which are Short And Giant Ragweed Pollen Mix UNII Codes?

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

  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (Active Moiety)

Which are Short And Giant Ragweed Pollen 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:

What is the NDC to RxNorm Crosswalk for Short And Giant Ragweed Pollen Mix?

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: 896138 - short ragweed pollen extract 50 MG/ML Injectable Solution
  • RxCUI: 896138 - Ambrosia artemisiifolia pollen extract 0.05 GM/ML Injectable Solution
  • RxCUI: 896138 - Ambrosia artemisiifolia pollen extract 50 MG/ML Injectable Solution
  • RxCUI: 899534 - giant ragweed pollen extract 25 MG/ML / short ragweed pollen extract 25 MG/ML Injectable Solution
  • RxCUI: 899534 - giant ragweed pollen extract 25 MG/ML / western ragweed pollen extract 25 MG/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".