Outdoor Explorer Set
NDC Package 59062-5300-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Outdoor Explorer Set is apply liberally 15 minutes before sun exposurereapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hourschildren under 6 months of age: ask a doctorSun Protection Measures. Marketed by Kas Direct Llc Dba Babyganics, this product is identified by NDC 59062-5300 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
59062-5300-1
Package Description
1 KIT in 1 PACKAGE * 59 mL in 1 TUBE (59062-1000-2) * 177 mL in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
59062530001

Clinical Specifications

Proprietary Name
Outdoor Explorer Set
Dosage Form
-
Usage Information
Apply liberally 15 minutes before sun exposurereapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hourschildren under 6 months of age: ask a doctorSun 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 10 a.m.-2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses

Regulatory & Marketing

Labeler Name
Kas Direct Llc Dba Babyganics
FDA Application #
part352
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
01-01-2018
Listing Expiration
12-31-2022
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 59062-5300-1 identifies a specific commercial package of 1 kit in 1 package * 59 ml in 1 tube (59062-1000-2) * 177 ml in 1 bottle, spray of Outdoor Explorer Set, labeled by Kas Direct Llc Dba Babyganics. 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 Kas Direct Llc Dba Babyganics on January 01, 2018. The current certification is valid through December 31, 2022.

How is this Kas Direct Llc Dba Babyganics product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59062530001. 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 (5-4-1)
59062-5300-1
11-Digit CMS (5-4-2)
59062-5300-01

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