NDC Package 82240-223-00 Dermaka Broad Spectrum Spf-42 Sunscreen

Titanium Dioxide,Zinc Oxide Cream Topical - View Billable Units, 11-Digit Format, RxNorm

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:
82240-223-00
Package Description:
100 mL in 1 TUBE
Product Code:
Proprietary Name:
Dermaka Broad Spectrum Spf-42 Sunscreen
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Apply liberally 15 minutes before sun exposure.Children under 6 months of age: ask a doctor.Reapply:afte 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m.Wear long-sleeved shirts, pants, hats and sunglasses.
11-Digit NDC Billing Format:
82240022300
Product Type:
Human Otc Drug
Labeler Name:
Dermaka Skin Products
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.
  • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-21-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 82240-223-00?

    The NDC Packaged Code 82240-223-00 is assigned to a package of 100 ml in 1 tube of Dermaka Broad Spectrum Spf-42 Sunscreen, a human over the counter drug labeled by Dermaka Skin Products. The product's dosage form is cream and is administered via topical form.

    Is NDC 82240-223 included in the NDC Directory?

    Yes, Dermaka Broad Spectrum Spf-42 Sunscreen with product code 82240-223 is active and included in the NDC Directory. The product was first marketed by Dermaka Skin Products on September 21, 2021 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 82240-223-00?

    The 11-digit format is 82240022300. 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
    5-3-282240-223-005-4-282240-0223-00