Sun Buff Spf 30 Mineral Sunscreen Powder
NDC Package 58274-030-01

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

Package Information

Sun Buff Spf 30 Mineral Sunscreen (zinc oxide/titanium dioxide) powders is apply liberally 15 minutes before sub exposure and as neededReapply: After 80 minutes of swimming or sweating; Immediately after towel drying; At least every 2 hoursSub Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. This formulation utilizes a powder delivery system. Marketed by Spf Ventures, Llc, this product is identified by NDC 58274-030 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
58274-030-01
Package Description
4 g in 1 TUBE
Product Code
58274-030
11-Digit Billing Format
58274003001

Clinical Specifications

Proprietary Name
Sun Buff Spf 30 Mineral Sunscreen
Non-Proprietary Name
Zinc Oxide/titanium Dioxide
Substance Name
Titanium Dioxide; Zinc Oxide
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
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)
Usage Information
Apply liberally 15 minutes before sub exposure and as neededReapply: After 80 minutes of swimming or sweating; Immediately after towel drying; At least every 2 hoursSub Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10am-2pm; Wear long-sleeved shirts, pants, hats and sunglasses; Children under 6 months of age: ask a doctor

Regulatory & Marketing

Labeler Name
Spf Ventures, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-24-2025
Listing Expiration
12-31-2026
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 58274-030-01 identifies a specific commercial package of 4 g in 1 tube of Sun Buff Spf 30 Mineral Sunscreen, a human over the counter drug labeled by Spf Ventures, Llc. This powder is formulated for topical use and contains titanium dioxide; 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 Spf Ventures, Llc on September 24, 2025. The current certification is valid through December 31, 2026.

How is this Spf Ventures, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 58274003001. 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)
58274-030-01
11-Digit CMS (5-4-2)
58274-0030-01

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