Rapid Relief Patch
NDC Package 83569-014-01
Package Information
Rapid Relief (plantar fasciitis pain relief lidocaine 4% menthol 1%) patches is adults and children 12 years of age and older:Clean and dry affected areaRemove film from patch and apply sticky side to desired areaApply patch to affected area not more than 3 times dailyDo not leave on skin for more than a total of 8 hours per dayCan be cut for custom sizing of pain areaChildren under 12 years of age: Do not use, consult a doctorSupervise children when they use this product. This formulation utilizes a patch delivery system. Marketed by Rapid Aid Viet Nam Company Limited, this product is identified by NDC 83569-014 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1249758 - lidocaine 4 % / menthol 1 % Medicated Patch
- RxCUI: 1249758 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch
Clinical Specifications
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
- Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
- Amides - [CS]
- Antiarrhythmic - [EPC] (Established Pharmacologic Class)
- Local Anesthesia - [PE] (Physiologic Effect)
- Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
- Amides - [CS]
- Antiarrhythmic - [EPC] (Established Pharmacologic Class)
- Local Anesthesia - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 83569 - Rapid Aid Viet Nam Company Limited
- 83569-014 - Rapid Relief
- 83569-014-01 - 100 g in 1 POUCH
- 83569-014 - Rapid 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.
* 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 (83569-014). 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 83569-014-01 identifies a specific commercial package of 100 g in 1 pouch of Rapid Relief, a human over the counter drug labeled by Rapid Aid Viet Nam Company Limited. This patch is formulated for topical use and contains lidocaine; menthol 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 Rapid Aid Viet Nam Company Limited on November 11, 2025. The current certification is valid through December 31, 2026.
How is this Rapid Aid Viet Nam Company Limited product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 83569001401. 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.