Skin Barista Rice Bran Cleansing Foam Liquid
NDC Package 70441-0002-1

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

Package Information

Skin Barista Rice Bran Cleansing Foam (allantoin) liquids is apply proper amount to the skin. This formulation utilizes a liquid delivery system. Marketed by Pioom Cosmetic Co.,ltd, this product is identified by NDC 70441-0002 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
70441-0002-1
Package Description
500 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
70441000201

Clinical Specifications

Proprietary Name
Skin Barista Rice Bran Cleansing Foam
Non-Proprietary Name
Allantoin
Substance Name
Allantoin
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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
Apply proper amount to the skin

Regulatory & Marketing

Labeler Name
Pioom Cosmetic Co.,ltd
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-04-2016
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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 70441-0002-1 identifies a specific commercial package of 500 ml in 1 bottle of Skin Barista Rice Bran Cleansing Foam, a human over the counter drug labeled by Pioom Cosmetic Co.,ltd. This liquid is formulated for topical use and contains allantoin 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 Pioom Cosmetic Co.,ltd on February 04, 2016. The current certification is valid through December 31, 2026.

How is this Pioom Cosmetic Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70441000201. 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)
70441-0002-1
11-Digit CMS (5-4-2)
70441-0002-01

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