NDC Package 79903-210-06 All Day Moisturizing Spf 15 Eqb

Octinoxate 6% Zinc Oxide 3% Lotion 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:
79903-210-06
Package Description:
1 CONTAINER in 1 CARTON / 177 mL in 1 CONTAINER
Product Code:
Proprietary Name:
All Day Moisturizing Spf 15 Eqb
Non-Proprietary Name:
Octinoxate 6% Zinc Oxide 3%
Substance Name:
Octinoxate; Zinc Oxide
Usage Information:
• apply liberal 15 minutes before sun exposure• reapply at least every 2 hours •use a water resistant sunscreen if swimmingor sweating•children under 6 months of age: ask a doctor• Sun Protection Measures:Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk. regularly usea sunscreen wrtha Broad Spectrum SPF value of15 or higher and other suncrin protection measures including: • limrt time in the sun, especial from 10a.m. -2 p.rn.•wear long-sleeve shorts , pants, hats and sunglasses
11-Digit NDC Billing Format:
79903021006
Product Type:
Human Otc Drug
Labeler Name:
Walmart
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.
  • Sample Package:
    No
    FDA Application Number:
    M006
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-09-2023
    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 79903-210-06?

    The NDC Packaged Code 79903-210-06 is assigned to a package of 1 container in 1 carton / 177 ml in 1 container of All Day Moisturizing Spf 15 Eqb, a human over the counter drug labeled by Walmart. The product's dosage form is lotion and is administered via topical form.

    Is NDC 79903-210 included in the NDC Directory?

    Yes, All Day Moisturizing Spf 15 Eqb with product code 79903-210 is active and included in the NDC Directory. The product was first marketed by Walmart on August 09, 2023 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 79903-210-06?

    The 11-digit format is 79903021006. 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
    5-3-279903-210-065-4-279903-0210-06