Sun Goo Mineral Sun Stick
NDC Package 82395-001-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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 inactivated by the FDA.

Sun Goo Mineral Sun Stick is apply generously and evenly 15 minutes before sun exposure Children under 6 months of age ask a doctor Sun protection measures reapply after 40 minutes of swimming or sweating, immediately after towel drying, at least every two hours, spending time in the sun increases your risk of skin cancer and early skin aging. Marketed by Sun Goo Inc, this product is identified by NDC 82395-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
82395-001-01
Package Description
1 TUBE in 1 CARTON / 15 mL in 1 TUBE
Product Code
82395-001
11-Digit Billing Format
82395000101

Clinical Specifications

Proprietary Name
Sun Goo Mineral Sun Stick
Dosage Form
-
Usage Information
Apply generously and evenly 15 minutes before sun exposure Children under 6 months of age ask a doctor Sun protection measures reapply after 40 minutes of swimming or sweating, immediately after towel drying, at least every two hours, spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this 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 10:00 a.m. – 2:00 p.m. wear long-sleeved shirts, pants, hats and sunglasses.

Regulatory & Marketing

Labeler Name
Sun Goo Inc
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
11-18-2021
Listing Expiration
12-31-2023
Exclude Flag
I
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 82395-001-01 identifies a specific commercial package of 1 tube in 1 carton / 15 ml in 1 tube of Sun Goo Mineral Sun Stick, labeled by Sun Goo Inc. 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 Sun Goo Inc on November 18, 2021. The current certification is valid through December 31, 2023.

How is this Sun Goo Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82395000101. 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)
82395-001-01
11-Digit CMS (5-4-2)
82395-0001-01

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