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  5. NDC Package Code: 22840-5720-5 Cranberry

NDC Package 22840-5720-5 Cranberry

Vaccinium Macrocarpon Solution Intradermal; Percutaneous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
22840-5720-5
Package Description:
5 mL in 1 BOTTLE, DROPPER
Product Code:
22840-5720
Proprietary Name:
Cranberry
Non-Proprietary Name:
Vaccinium Macrocarpon
Substance Name:
Cranberry
Usage Information:
Cranberry has been used for reducing the risk of "bladder infections" (urinary tract infections). It has also been used for decreasing the smell of urine in people who are unable to control urination (incontinent). This product should not be used alone to treat bladder infections. It may not work, and the delay could allow the infection to worsen. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
11-Digit NDC Billing Format:
22840572005
NDC to RxNorm Crosswalk:
  • RxCUI: 1000013 - whole wheat allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1000013 - whole wheat allergenic extract 0.05 GM/ML Injectable Solution
  • RxCUI: 1000013 - whole wheat extract 50 MG/ML Injectable Solution
  • RxCUI: 1006349 - pork allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1006349 - pork extract 0.05 GM/ML Injectable Solution
    • Product Type:
    Non-standardized Allergenic
    Labeler Name:
    Greer Laboratories, Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Intradermal - Administration within the dermis.
  • Percutaneous - Administration through the skin.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • CRANBERRY .025 g/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Fruit Proteins - [EXT]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
    • Sample Package:
    No
    FDA Application Number:
    BLA101833
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    09-15-1981
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    22840-5720-210 mL in 1 VIAL, MULTI-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 22840-5720-5?

    The NDC Packaged Code 22840-5720-5 is assigned to a package of 5 ml in 1 bottle, dropper of Cranberry, a non-standardized allergenic label labeled by Greer Laboratories, Inc.. The product's dosage form is solution and is administered via intradermal; percutaneous; subcutaneous form.

    Is NDC 22840-5720 included in the NDC Directory?

    Yes, Cranberry with product code 22840-5720 is active and included in the NDC Directory. The product was first marketed by Greer Laboratories, Inc. on September 15, 1981 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 22840-5720-5?

    The 11-digit format is 22840572005. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-122840-5720-55-4-222840-5720-05