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  5. NDC Package Code: 75936-250-01 Sunnyscreen Spf 50

NDC Package 75936-250-01 Sunnyscreen Spf 50

Titanium Dioxide,Zinc Oxide 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:
75936-250-01
Package Description:
89 mL in 1 BOTTLE
Product Code:
75936-250
Proprietary Name:
Sunnyscreen Spf 50
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Stop use and ask a doctor if rash occurs or irritation develops and lasts.
11-Digit NDC Billing Format:
75936025001
Product Type:
Human Otc Drug
Labeler Name:
Supergoop, Llc
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):
  • TITANIUM DIOXIDE 3.4 g/100mL
  • ZINC OXIDE 23.8 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-01-2019
    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 75936-250-01?

    The NDC Packaged Code 75936-250-01 is assigned to a package of 89 ml in 1 bottle of Sunnyscreen Spf 50, a human over the counter drug labeled by Supergoop, Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 75936-250 included in the NDC Directory?

    Yes, Sunnyscreen Spf 50 with product code 75936-250 is active and included in the NDC Directory. The product was first marketed by Supergoop, Llc on April 01, 2019 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 75936-250-01?

    The 11-digit format is 75936025001. 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
    5-3-275936-250-015-4-275936-0250-01