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  5. NDC Package Code: 49546-105-03 Ivy-dry Super

NDC Package 49546-105-03 Ivy-dry Super

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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

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:
49546-105-03
Package Description:
89 mL in 1 CANISTER
Product Code:
49546-105
Proprietary Name:
Ivy-dry Super
Usage Information:
Apply to affected area not more than 3 times daily.Children under 6 years of age: do not use, ask a doctor.Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary. Test product on small patch of skin before applying to the entire body.
11-Digit NDC Billing Format:
49546010503
NDC to RxNorm Crosswalk:
  • RxCUI: 1302630 - benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % Topical Spray
  • RxCUI: 1302630 - benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical Spray
  • RxCUI: 1302633 - IVY DRY SUPER 10 % / 0.5 % / 0.25 % Topical Spray
  • RxCUI: 1302633 - benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical Spray [Ivy Dry Super Continuous Spray]
  • RxCUI: 1302633 - Ivy Dry Super Continuous Spray (benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % ) Topical Spray
    • Labeler Name:
    Ivy-dry, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-11-2012
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    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.

    Frequently Asked Questions

    What is NDC 49546-105-03?

    The NDC Packaged Code 49546-105-03 is assigned to a package of 89 ml in 1 canister of Ivy-dry Super, labeled by Ivy-dry, Inc.. The product's dosage form is and is administered via form.

    Is NDC 49546-105 included in the NDC Directory?

    No, Ivy-dry Super with product code 49546-105 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Ivy-dry, Inc. on July 11, 2012 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49546-105-03?

    The 11-digit format is 49546010503. 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 5-3-2 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
    5-3-249546-105-035-4-249546-0105-03