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  5. NDC Package Code: 87044-1201-1 Seye

NDC Package 87044-1201-1 Seye

Zinc Oxide And Titanium Dioxide Cream Cream Topical - 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:
87044-1201-1
Package Description:
1 g in 1 CARTON
Product Code:
87044-1201
Proprietary Name:
Seye
Non-Proprietary Name:
Zinc Oxide And Titanium Dioxide Cream
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Apply liberally 15 minutes before sun exposureReapply at least every 2 hoursUse a water-resistant sunscreen if swimming or sweatingSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:​ 1. limit time in the sun, especially from 10 a.m. - 2 p.m. 2. Wear long-sleeved shirts, pants, hats, and sunglassesChildren under 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
87044120101
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Seye Biomedical Technology Co., Ltd.
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
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):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-21-2025
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 87044-1201-1?

The NDC Packaged Code 87044-1201-1 is assigned to a package of 1 g in 1 carton of Seye, a human over the counter drug labeled by Guangzhou Seye Biomedical Technology Co., Ltd.. The product's dosage form is cream and is administered via topical form.

Is NDC 87044-1201 included in the NDC Directory?

Yes, Seye with product code 87044-1201 is active and included in the NDC Directory. The product was first marketed by Guangzhou Seye Biomedical Technology Co., Ltd. on August 21, 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 87044-1201-1?

The 11-digit format is 87044120101. 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 5-4-1 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
5-4-187044-1201-15-4-287044-1201-01