Wildara Mineral Tallow Sunscreen Spf 50
NDC Package 87761-005-01

11-digit billing NDC: 87761000501
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Wildara Mineral Tallow Sunscreen Spf 50 is directions shake well prior to useapply lberally 15 minutes before sun exposure .children under 6 months of age: Ask a doctorreapply:.after 80 minutes of swimming or sweating. Marketed by Moes Group Llc, this product is identified by NDC 87761-005 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
87761-005-01
Package Description
100 g in 1 BOTTLE
Product Code
87761-005
11-Digit Billing Format
87761000501

Clinical Specifications

Proprietary Name
Wildara Mineral Tallow Sunscreen Spf 50
Dosage Form
-
Usage Information
Directions shake well prior to useapply lberally 15 minutes before sun exposure .children under 6 months of age: Ask a doctorreapply:.after 80 minutes of swimming or sweating

Regulatory & Marketing

Labeler Name
Moes Group Llc
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-14-2026
End Marketing Date
08-22-2026
Listing Expiration
08-22-2026
Exclude Flag
D
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 87761-005-01 identifies a specific commercial package of 100 g in 1 bottle of Wildara Mineral Tallow Sunscreen Spf 50, labeled by Moes Group Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Moes Group Llc on June 14, 2026. The current certification is valid through August 22, 2026.

How is this Moes Group Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87761000501. 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)
87761-005-01
11-Digit CMS (5-4-2)
87761-0005-01

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