Menow Sunscreen Powder
NDC Package 85138-101-02

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

Package Information

Menow Sunscreen (ethylhexyl methoxycinnamate, bis-ethylhexyloxyphenol methoxyphenyl triazine, zinc oxide, titanium dioxide) powders is indications & usage section:SUNSCREEN PRESSED POWDER,SETTING MAKEUP WHILE PROTECTING AGAINST UVA/UVB. This formulation utilizes a powder delivery system. Marketed by Shantou Qiwei Industry Co.,ltd, this product is identified by NDC 85138-101.

Identification & Billing

NDC Package Code
85138-101-02
Package Description
1 BOX in 1 BOX / 9 g in 1 BOX (85138-101-01)
Product Code
85138-101
11-Digit Billing Format
85138010102

Clinical Specifications

Proprietary Name
Menow Sunscreen
Non-Proprietary Name
Ethylhexyl Methoxycinnamate, Bis-ethylhexyloxyphenol Methoxyphenyl Triazine, Zinc Oxide, Titanium Dioxide
Substance Name
Bis-ethylhexyloxyphenol Methoxyphenyl Triazine; Ethylhexyl Methoxycinnamate; Titanium Dioxide; 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
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
Indications & usage section:SUNSCREEN PRESSED POWDER,SETTING MAKEUP WHILE PROTECTING AGAINST UVA/UVB

Regulatory & Marketing

Labeler Name
Shantou Qiwei Industry Co.,ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
01-17-2025
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 85138-101-02 identifies a specific commercial package of 1 box in 1 box / 9 g in 1 box (85138-101-01) of Menow Sunscreen, a human over the counter drug labeled by Shantou Qiwei Industry Co.,ltd. This powder is formulated for cutaneous use and contains bis-ethylhexyloxyphenol methoxyphenyl triazine; ethylhexyl methoxycinnamate; titanium dioxide; 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 Shantou Qiwei Industry Co.,ltd on January 17, 2025. The current certification is valid through December 31, 2026.

How is this Shantou Qiwei Industry Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85138010102. 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)
85138-101-02
11-Digit CMS (5-4-2)
85138-0101-02

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