Medicated Body Powder
NDC Package 52000-038-26

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

Package Information

Medicated Body (menthol and zinc oxide) powders is adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times dailyChildren under 2 years of age: consult a doctorFor best results, dry area thoroughly before applying. This formulation utilizes a powder delivery system. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-038 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
52000-038-26
Package Description
226 g in 1 BOTTLE
Product Code
11-Digit Billing Format
52000003826
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
Non-Proprietary Name
Menthol And Zinc Oxide
Substance Name
Menthol, Unspecified Form; Zinc Oxide
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Usage Information
Adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times dailyChildren under 2 years of age: consult a doctorFor best results, dry area thoroughly before applying

Regulatory & Marketing

Labeler Name
Universal Distribution Center Llc
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-04-2017
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (52000-038). Click a package code to view its specific billing and regulatory data.

283 g in 1 BOTTLE

* 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 52000-038-26 identifies a specific commercial package of 226 g in 1 bottle of Medicated Body, a human over the counter drug labeled by Universal Distribution Center Llc. This powder is formulated for topical use and contains menthol, unspecified form; zinc oxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Universal Distribution Center Llc on December 04, 2017. The current certification is valid through December 31, 2026.

How is this Universal Distribution Center Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52000003826. 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)
52000-038-26
11-Digit CMS (5-4-2)
52000-0038-26

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