Medicated Body
NDC Package 49348-834-92

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.

Medicated Body is uses for temporary relief of pain and itching due to:•minor cuts      •sunburn           •insect bites•poison ivy       •poison oak      •poison sumac•scrapes            •minor burns    •minor skin irritationsdries the oozing and weeping of:•poison ivy       •poison oak      •poison sumac. Marketed by Mckesson, this product is identified by NDC 49348-834 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
49348-834-92
Package Description
.283 kg in 1 BOTTLE, PLASTIC
Product Code
49348-834
11-Digit Billing Format
49348083492
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
283.000 GM
RxNorm Crosswalk
  • RxCUI: 577232 - menthol 0.15 % / zinc oxide 1 % Topical Powder
  • RxCUI: 577232 - menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical Powder
  • RxCUI: 577232 - Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical Powder

Clinical Specifications

Proprietary Name
Medicated Body
Dosage Form
-
Usage Information
Uses for temporary relief of pain and itching due to:•minor cuts      •sunburn           •insect bites•poison ivy       •poison oak      •poison sumac•scrapes            •minor burns    •minor skin irritationsdries the oozing and weeping of:•poison ivy       •poison oak      •poison sumac

Regulatory & Marketing

Labeler Name
Mckesson
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
06-18-1994
Listing Expiration
12-31-2018
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 49348-834-92 identifies a specific commercial package of .283 kg in 1 bottle, plastic of Medicated Body, labeled by Mckesson. 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 Mckesson on June 18, 1994. The current certification is valid through December 31, 2018.

How is this Mckesson product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348083492. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 283.000 total billable units per package. 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)
49348-834-92
11-Digit CMS (5-4-2)
49348-0834-92

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