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  5. NDC Package Code: 85138-101-02 Menow Sunscreen

NDC Package 85138-101-02 Menow Sunscreen

Ethylhexyl Methoxycinnamate,Bis-ethylhexyloxyphenol Methoxyphenyl Triazine,Zinc - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

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
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
Usage Information:
Indications & usage section:SUNSCREEN PRESSED POWDER,SETTING MAKEUP WHILE PROTECTING AGAINST UVA/UVB
11-Digit NDC Billing Format:
85138010102
Product Type:
Human Otc Drug
Labeler Name:
Shantou Qiwei Industry Co.,ltd
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(s):
Cutaneous - Administration to the skin.
Active Ingredient(s):
Sample Package:
No
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 Date:
12-31-2026
Exclude Flag:
N
Code 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 disclaimer below.

Frequently Asked Questions

What is NDC 85138-101-02?

The NDC Packaged Code 85138-101-02 is assigned to a 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. The product's dosage form is powder and is administered via cutaneous form.

Is NDC 85138-101 included in the NDC Directory?

Yes, Menow Sunscreen with product code 85138-101 is active and included in the NDC Directory. The product was first marketed by Shantou Qiwei Industry Co.,ltd on January 17, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85138-101-02?

The 11-digit format is 85138010102. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-285138-101-025-4-285138-0101-02