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  5. NDC Package Code: 85053-003-01 Woodsleep Tallow Sunscreen

NDC Package 85053-003-01 Woodsleep Tallow Sunscreen

Titanium Dioxide 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:
85053-003-01
Package Description:
60 mg in 1 BOX
Product Code:
85053-003
Proprietary Name:
Woodsleep Tallow Sunscreen
Non-Proprietary Name:
Titanium Dioxide
Substance Name:
Tallow
Usage Information:
This product is used as 1. Effectively block ultraviolet rays, build a natural protective barrier for the skin, and protect against the sun with peace of mind.2. The unique formula deeply moisturizes and lasts for a long time, preventing the skin from drying out due to sun exposure, and keeping the skin moisturized and tender.3. The soothing formula reduces skin irritation, relieves discomfort after sun exposure, and gives gentle care to the skin, suitable for all skin types.
11-Digit NDC Billing Format:
85053000301
Product Type:
Human Otc Drug
Labeler Name:
Shantou Woodsleep Biotechnology 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):
TALLOW .012 mg/60mg
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-28-2025
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 85053-003-01?

The NDC Packaged Code 85053-003-01 is assigned to a package of 60 mg in 1 box of Woodsleep Tallow Sunscreen, a human over the counter drug labeled by Shantou Woodsleep Biotechnology Co., Ltd.. The product's dosage form is cream and is administered via topical form.

Is NDC 85053-003 included in the NDC Directory?

Yes, Woodsleep Tallow Sunscreen with product code 85053-003 is active and included in the NDC Directory. The product was first marketed by Shantou Woodsleep Biotechnology Co., Ltd. on April 28, 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 85053-003-01?

The 11-digit format is 85053000301. 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
5-3-285053-003-015-4-285053-0003-01