Coretex Professional Outdoor Skin Protection Wallet Refill
NDC Package 65753-515-36
Package Information
Coretex Professional Outdoor Skin Protection Wallet Refill is put enough product in your palm to cover hands and rub hands together briskly until dry. Marketed by Coretex Products Inc, this product is identified by NDC 65753-515 and is authorized under FDA application M020.
Identification & Billing
- RxCUI: 1039474 - ethanol 62.5 % Topical Solution
- RxCUI: 1039474 - ethanol 0.625 ML/ML Topical Solution
- RxCUI: 1043353 - benzocaine 6 % Medicated Pad
- RxCUI: 1043353 - benzocaine 60 MG/ML Medicated Pad
- RxCUI: 1043353 - benzocaine 6 % Medicated Wipe
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 65753 - Coretex Products Inc
- 65753-515 - Coretex Professional Outdoor Skin Protection Wallet Refill
- 65753-515-36 - 1 KIT in 1 KIT * 4.44 mL in 1 APPLICATOR (65753-108-39) * 1.1 mL in 1 POUCH * 1 mL in 1 POUCH (65753-400-39) * 3.5 mL in 1 POUCH * 7 g in 1 POUCH (65753-109-39) * 44 mL in 1 PACKET (65753-110-37)
- 65753-515 - Coretex Professional Outdoor Skin Protection Wallet Refill
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 65753-515-36 identifies a specific commercial package of 1 kit in 1 kit * 4.44 ml in 1 applicator (65753-108-39) * 1.1 ml in 1 pouch * 1 ml in 1 pouch (65753-400-39) * 3.5 ml in 1 pouch * 7 g in 1 pouch (65753-109-39) * 44 ml in 1 packet (65753-110-37) of Coretex Professional Outdoor Skin Protection Wallet Refill, labeled by Coretex Products 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 Coretex Products Inc on February 24, 2023. The current certification is valid through December 31, 2024.
How is this Coretex Products Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 65753051536. 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.