Medicated Cornstarch Baby Powder
NDC Package 42669-231-04

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Medicated Cornstarch Baby Powder (active corn starch) powders is babies: Change wet and soiled diaper promptly, cleanse the diaper area and allow to dry. This formulation utilizes a powder delivery system. Marketed by Davion, Inc., this product is identified by NDC 42669-231 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
42669-231-04
Package Description
113 g in 1 BOX
Product Code
42669-231
11-Digit Billing Format
42669023104
RxNorm Crosswalk
  • RxCUI: 1361201 - cornstarch 79 % / kaolin 4 % / zinc oxide 15 % Topical Powder
  • RxCUI: 1361201 - corn starch 0.79 MG/MG / kaolin 0.04 MG/MG / zinc oxide 0.15 MG/MG Topical Powder
  • RxCUI: 1361201 - corn starch 0.79 MG/MG / Kaolin 0.04 MG/MG / ZNO 0.15 MG/MG Topical Powder

Clinical Specifications

Proprietary Name
Medicated Cornstarch Baby Powder
Non-Proprietary Name
Active Corn Starch
Substance Name
Kaolin; Starch, Corn; 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.
Active Ingredient(s)
Usage Information
Babies: Change wet and soiled diaper promptly, cleanse the diaper area and allow to dry.  Apply powder liberally as often as necessary, with each diaper change, especially at bedtime, or anytime when exposure to wet diapers may be prolonged.  Apply powder close to the body away from child's face.  Carefully shake the powder into the diaper or into the hand and apply to diaper area.  Adults and children 2 years and older: apply freely up to 3 or 4 times daily.  For best results, dry skin thoroughly before applying.

Regulatory & Marketing

Labeler Name
Davion, Inc.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2016
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 42669-231-04 identifies a specific commercial package of 113 g in 1 box of Medicated Cornstarch Baby Powder, a human over the counter drug labeled by Davion, Inc.. This powder is formulated for topical use and contains kaolin; starch, corn; 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 Davion, Inc. on September 01, 2016. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42669023104. 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)
42669-231-04
11-Digit CMS (5-4-2)
42669-0231-04

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