NDC Package 82281-239-00 Stryx Daily Moisturizer Spf-30

Octisalate,Ensulizole 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:
82281-239-00
Package Description:
100 mL in 1 TUBE
Product Code:
Proprietary Name:
Stryx Daily Moisturizer Spf-30
Non-Proprietary Name:
Octisalate, Ensulizole
Substance Name:
Ensulizole; Octisalate
Usage Information:
- Apply liberally 15 minutes before sun exposure- Children under 6 months of age: ask a doctor - Reapply: at least every 2 hours- Sun 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:
82281023900
Product Type:
Human Otc Drug
Labeler Name:
Stryx Men, Inc.
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:
    10-10-2021
    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.

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    Frequently Asked Questions

    What is NDC 82281-239-00?

    The NDC Packaged Code 82281-239-00 is assigned to a package of 100 ml in 1 tube of Stryx Daily Moisturizer Spf-30, a human over the counter drug labeled by Stryx Men, Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 82281-239 included in the NDC Directory?

    Yes, Stryx Daily Moisturizer Spf-30 with product code 82281-239 is active and included in the NDC Directory. The product was first marketed by Stryx Men, Inc. on October 10, 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 82281-239-00?

    The 11-digit format is 82281023900. 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
    5-3-282281-239-005-4-282281-0239-00