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  5. NDC Package Code: 83872-012-01 Face Sunscreen Skin Care

NDC Package 83872-012-01 Face Sunscreen Skin Care

Face Sunscreen 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:
83872-012-01
Package Description:
50 g in 1 BOTTLE
Product Code:
83872-012
Proprietary Name:
Face Sunscreen Skin Care
Non-Proprietary Name:
Face Sunscreen
Substance Name:
Octinoxate; Octocrylene; Zinc Oxide
Usage Information:
Directions for use -apply liberally 15 minutes before sun exposure. -reapply at least every 2 hours. -use a water resistant sunscreen if swimming or sweating. -Sun 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 B road. -Spectrum SPF value of15 or higher and other sun protection： -limit time in the sun, especially from 10 a.m.-2 p.m. -and wear long-sleeved shirts, pants, hats, and sunglasses
11-Digit NDC Billing Format:
83872001201
Product Type:
Human Otc Drug
Labeler Name:
Shenzhen Xiaomai Manufacturing 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):
  • OCTINOXATE 5 g/100g
  • OCTOCRYLENE 5 g/100g
  • ZINC OXIDE 6.2 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-29-2024
    Listing Expiration Date:
    12-31-2025
    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 83872-012-01?

    The NDC Packaged Code 83872-012-01 is assigned to a package of 50 g in 1 bottle of Face Sunscreen Skin Care, a human over the counter drug labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. The product's dosage form is cream and is administered via topical form.

    Is NDC 83872-012 included in the NDC Directory?

    Yes, Face Sunscreen Skin Care with product code 83872-012 is active and included in the NDC Directory. The product was first marketed by Shenzhen Xiaomai Manufacturing Co., Ltd. on January 29, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 83872-012-01?

    The 11-digit format is 83872001201. 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
    5-3-283872-012-015-4-283872-0012-01