Ivy Dry
NDC Package 49546-201-28

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Ivy Dry is apply to affected area not more than 3 times daily.Children under 2 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. Marketed by Ivy Dry, Inc., this product is identified by NDC 49546-201 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
49546-201-28
Package Description
1 TUBE in 1 BOX / 28 g in 1 TUBE
Product Code
49546-201
11-Digit Billing Format
49546020128
RxNorm Crosswalk
  • RxCUI: 1305913 - benzyl alcohol 10 % / camphor 0.6 % / menthol 0.4 % Topical Cream
  • RxCUI: 1305913 - benzyl alcohol 100 MG/ML / camphor 6 MG/ML / menthol 4 MG/ML Topical Cream
  • RxCUI: 1305916 - Ivy-Dry Cream 10 % / 0.6 % / 0.4 % Topical Cream
  • RxCUI: 1305916 - benzyl alcohol 100 MG/ML / camphor 6 MG/ML / menthol 4 MG/ML Topical Cream [Ivy-Dry Cream]
  • RxCUI: 1305916 - Ivy-Dry Cream (benzyl alcohol 10 % / camphor 0.6 % / menthol 0.4 % ) Topical Cream

Clinical Specifications

Proprietary Name
Ivy Dry
Dosage Form
-
Usage Information
Apply to affected area not more than 3 times daily.Children under 2 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.

Regulatory & Marketing

Labeler Name
Ivy Dry, Inc.
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
08-22-2012
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 49546-201-28 identifies a specific commercial package of 1 tube in 1 box / 28 g in 1 tube of Ivy Dry, labeled by Ivy Dry, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Ivy Dry, Inc. on August 22, 2012. The current certification is valid through December 31, 2021.

How is this Ivy Dry, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49546020128. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
49546-201-28
11-Digit CMS (5-4-2)
49546-0201-28

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.