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  5. NDC Package Code: 73071-101-01 Dewytree Urban Shade Hyaluronic Lightweight Sunscreen

NDC Package 73071-101-01 Dewytree Urban Shade Hyaluronic Lightweight Sunscreen

Octocrylene,Homosalate,Octisalate,Avobenzone 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:
73071-101-01
Package Description:
1 TUBE in 1 BOX / 50 mL in 1 TUBE (73071-101-02)
Product Code:
73071-101
Proprietary Name:
Dewytree Urban Shade Hyaluronic Lightweight Sunscreen
Non-Proprietary Name:
Octocrylene, Homosalate, Octisalate, Avobenzone
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
■ Helps prevent sunburn. ■ if used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
11-Digit NDC Billing Format:
73071010101
Product Type:
Human Otc Drug
Labeler Name:
Dewytree 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:
03-26-2025
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 73071-101-01?

The NDC Packaged Code 73071-101-01 is assigned to a package of 1 tube in 1 box / 50 ml in 1 tube (73071-101-02) of Dewytree Urban Shade Hyaluronic Lightweight Sunscreen, a human over the counter drug labeled by Dewytree Co. ,ltd. The product's dosage form is cream and is administered via topical form.

Is NDC 73071-101 included in the NDC Directory?

Yes, Dewytree Urban Shade Hyaluronic Lightweight Sunscreen with product code 73071-101 is active and included in the NDC Directory. The product was first marketed by Dewytree Co. ,ltd on March 26, 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 73071-101-01?

The 11-digit format is 73071010101. 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
5-3-273071-101-015-4-273071-0101-01