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

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

All Day Moisturizing Spf 15 (octinoxate 6% zinc oxide 3%) lotions is • 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. This formulation utilizes a lotion delivery system. Marketed by Walmart, this product is identified by NDC 79903-210 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
79903-210-06
Package Description
1 CONTAINER in 1 CARTON / 177 mL in 1 CONTAINER
Product Code
79903-210
11-Digit Billing Format
79903021006

Clinical Specifications

Proprietary Name
All Day Moisturizing Spf 15 Eqb
Non-Proprietary Name
Octinoxate 6% Zinc Oxide 3%
Substance Name
Octinoxate; Zinc Oxide
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
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)
Pharmacologic Class
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

Regulatory & Marketing

Labeler Name
Walmart
Product Type
Human Otc Drug
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-09-2023
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 79903-210-06 identifies a specific commercial 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. This lotion is formulated for topical use and contains octinoxate; zinc oxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Walmart on August 09, 2023. The current certification is valid through December 31, 2027.

How is this Walmart product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79903021006. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
79903-210-06
11-Digit CMS (5-4-2)
79903-0210-06

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.