Personal Care
NDC Package 29500-9090-1

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.

Personal Care is a medication used as Uses     for the temporary relief of the pain and itch associated with:- minor cuts - scrapes - sunburn - insect bites - prickly heat - rashes- minor burns - minor skin irritation - dries the oozing of poison ivy, oak and sumac. Marketed by Personal Care Products, Inc., this product is identified by NDC 29500-9090 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
29500-9090-1
Package Description
283 g in 1 BOTTLE
Product Code
29500-9090
11-Digit Billing Format
29500909001
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
Personal Care
Dosage Form
-
Usage Information
This product is used as Uses     for the temporary relief of the pain and itch associated with:- minor cuts - scrapes - sunburn - insect bites - prickly heat - rashes- minor burns - minor skin irritation - dries the oozing of poison ivy, oak and sumac.

Regulatory & Marketing

Labeler Name
Personal Care Products, 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
09-01-2009
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 29500-9090-1 identifies a specific commercial package of 283 g in 1 bottle of Personal Care, labeled by Personal Care Products, 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 Personal Care Products, Inc. on September 01, 2009. The current certification is valid through December 31, 2018.

How is this Personal Care Products, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 29500909001. 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 (5-4-1)
29500-9090-1
11-Digit CMS (5-4-2)
29500-9090-01

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