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  5. NDC Package Code: 82516-202-02 Sunscreen

NDC Package 82516-202-02 Sunscreen

Everyday Skin Tint Spf 30 Lotion 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:
82516-202-02
Package Description:
1 BOTTLE, PUMP in 1 CARTON / 30 g in 1 BOTTLE, PUMP (82516-202-01)
Product Code:
82516-202
Proprietary Name:
Sunscreen
Non-Proprietary Name:
Everyday Skin Tint Spf 30
Substance Name:
Zinc Oxide
Usage Information:
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
11-Digit NDC Billing Format:
82516020202
Product Type:
Human Otc Drug
Labeler Name:
True Botanicals
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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):
  • ZINC OXIDE 18 g/100g
    • Sample Package:
    No
    FDA Application Number:
    part352
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-16-2022
    Listing Expiration Date:
    12-31-2024
    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 82516-202-02?

    The NDC Packaged Code 82516-202-02 is assigned to a package of 1 bottle, pump in 1 carton / 30 g in 1 bottle, pump (82516-202-01) of Sunscreen, a human over the counter drug labeled by True Botanicals. The product's dosage form is lotion and is administered via topical form.

    Is NDC 82516-202 included in the NDC Directory?

    Yes, Sunscreen with product code 82516-202 is active and included in the NDC Directory. The product was first marketed by True Botanicals on June 16, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 82516-202-02?

    The 11-digit format is 82516020202. 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
    5-3-282516-202-025-4-282516-0202-02