Spf 50 Plus Sunscreen Stick
NDC Package 59062-1200-2
Package Information
Spf 50 Plus Sunscreen (titanium dioxide and zinc oxide) sticks is apply liberally and evenly 15 minutes before sun exposurereapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursthis product is meant for targeted protection and small areas of exposed skinfor full protection use in conjunction with another sunscreen lotion or spraychildren under 6 months of age: ask a doctorSun Protection Measures. This formulation utilizes a stick delivery system. Marketed by Kas Direct Llc Dba Babyganics, this product is identified by NDC 59062-1200 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 59062 - Kas Direct Llc Dba Babyganics
- 59062-1200 - Spf 50 Plus Sunscreen
- 59062-1200-2 - 2 APPLICATOR in 1 BLISTER PACK / 13 g in 1 APPLICATOR
- 59062-1200 - Spf 50 Plus Sunscreen
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (59062-1200). Click a package code to view its specific billing and regulatory data.
* 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 59062-1200-2 identifies a specific commercial package of 2 applicator in 1 blister pack / 13 g in 1 applicator of Spf 50 Plus Sunscreen All Mineral Active Ingredients, a human over the counter drug labeled by Kas Direct Llc Dba Babyganics. This stick 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 Kas Direct Llc Dba Babyganics on June 21, 2013. The current certification is valid through December 31, 2026.
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: 59062120002. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.