Wellpatch Cooling Pain Relief Patch
NDC Package 10742-8125-1
Package Information
Wellpatch Cooling Pain Relief (menthol) patches is •adults and children 12 years and over: apply to affected area; change patch 1 to 2 times daily•children under 12 years: ask a doctor•FOR BEST RESULTS apply to clean, dry skin•tear open pouch and remove patch; if desired, cut patch to size•grasp both ends of the patch firmly with thumbs near center•stretch patch until the backing separates•remove protective film while applying patch directly to site of pain. This formulation utilizes a patch delivery system. Marketed by The Mentholatum Company, this product is identified by NDC 10742-8125 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1232426 - WellPatch Backache Relief 5 % Medicated Patch
- RxCUI: 1232426 - menthol 0.05 MG/MG Medicated Patch [Wellpatch Backache Relief]
- RxCUI: 1232426 - Wellpatch Backache Relief 5 % Medicated Patch
- RxCUI: 420222 - menthol 5 % Medicated Patch
- RxCUI: 420222 - menthol 0.05 MG/MG Medicated Patch
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10742 - The Mentholatum Company
- 10742-8125 - Wellpatch Cooling Pain Relief
- 10742-8125-1 - 1 PATCH in 1 POUCH
- 10742-8125 - Wellpatch Cooling Pain Relief
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 10742-8125-1 identifies a specific commercial package of 1 patch in 1 pouch of Wellpatch Cooling Pain Relief, a human over the counter drug labeled by The Mentholatum Company. This patch is formulated for topical use and contains menthol, unspecified form 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 The Mentholatum Company on February 06, 2017. The current certification is valid through December 31, 2026.
How is this The Mentholatum Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10742812501. 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.