Coretex Sun X Spf 30 New Lotion
NDC Package 65753-110-35
Package Information
Coretex Sun X Spf 30 New (avobenzone, homosalate, octisalate, octocrylene) lotions is put enough product in your palm to cover hands and rub hands together briskly until dry. This formulation utilizes a lotion delivery system. Marketed by Coretex Products Inc, this product is identified by NDC 65753-110 and is authorized under FDA application M020.
Identification & Billing
- RxCUI: 1043353 - benzocaine 6 % Medicated Pad
- RxCUI: 1043353 - benzocaine 60 MG/ML Medicated Pad
- RxCUI: 1043353 - benzocaine 6 % Medicated Wipe
- RxCUI: 1043353 - benzocaine 6 % Topical Swab
- RxCUI: 2263166 - StingX 6 % Topical Swab
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 65753 - Coretex Products Inc
- 65753-110 - Coretex Sun X Spf 30 New
- 65753-110-35 - 751 mL in 1 BOTTLE
- 65753-110 - Coretex Sun X Spf 30 New
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 (65753-110). 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 65753-110-35 identifies a specific commercial package of 751 ml in 1 bottle of Coretex Sun X Spf 30 New, a human over the counter drug labeled by Coretex Products Inc. This lotion is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Coretex Products Inc on January 07, 2021. The current certification is valid through December 31, 2026.
How is this Coretex Products Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 65753011035. 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 Product segment to maintain the 5-4-2 structure.
