NDC Package 55910-726-10 Sunscreen

Octinoxate,Octisalate,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:
55910-726-10
Package Description:
28.3 g in 1 PACKAGE
Product Code:
Proprietary Name:
Sunscreen
Non-Proprietary Name:
Octinoxate, Octisalate, Zinc Oxide
Substance Name:
Octinoxate; Octisalate; Octocrylene; Zinc Oxide
Usage Information:
Directions■ apply liberally 15 minutes before sun exposure■ reapply:■ after 80 minutes of swimming or sweating■ immediately after towel drying■ at least every 2 hours■ Sun Protection Measures. Spending time in thesun increases your risk of skin cancer and earlyskin aging. To decrease this risk, regularly use asunscreen with a Broad Spectrum SPF value of15 or higher and other sun protectionmeasures including:■ limit time in the sun, especially from10 a.m. – 2 p.m.■ wear long-sleeved shirts, pants, hatsand sunglasses■ children under 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
55910072610
Product Type:
Human Otc Drug
Labeler Name:
Old East Main Co.
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:
    part352
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    10-01-2019
    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 55910-726-10?

    The NDC Packaged Code 55910-726-10 is assigned to a package of 28.3 g in 1 package of Sunscreen, a human over the counter drug labeled by Old East Main Co.. The product's dosage form is cream and is administered via topical form.

    Is NDC 55910-726 included in the NDC Directory?

    Yes, Sunscreen with product code 55910-726 is active and included in the NDC Directory. The product was first marketed by Old East Main Co. on October 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 55910-726-10?

    The 11-digit format is 55910072610. 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
    5-3-255910-726-105-4-255910-0726-10