N-labs Arcticzen Pain Relief Knee Patch
NDC Package 71856-356-30
Package Information
N-labs Arcticzen Pain Relief Knee (camphor (synthetic), menthol) patches is adults and children 12 years of age and older: ● clean and dry the affected area ● apply a patch at a time to the affected area; not more than 3 or 4 times daily to the affected area ● remove the patch from the skin after at most 8 hours of application. This formulation utilizes a patch delivery system. Marketed by Nutriomo Labs Pte., Ltd, this product is identified by NDC 71856-356 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 2699820 - camphor 3.5 % / menthol 6 % Medicated Patch
- RxCUI: 2699820 - camphor 0.035 MG/MG / menthol 0.06 MG/MG Medicated Patch
- RxCUI: 2699825 - ARCTICZEN 3.5 % / 6 % Medicated Patch
- RxCUI: 2699825 - camphor 0.035 MG/MG / menthol 0.06 MG/MG Medicated Patch [Arcticzen]
- RxCUI: 2699825 - Arcticzen (camphor 3.5 % / menthol 6 % ) Medicated Patch
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71856 - Nutriomo Labs Pte., Ltd
- 71856-356 - N-labs Arcticzen Pain Relief Knee
- 71856-356-30 - 15 PACKET in 1 BOX / 2 PATCH in 1 PACKET / 3 g in 1 PATCH
- 71856-356 - N-labs Arcticzen Pain Relief Knee
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 71856-356-30 identifies a specific commercial package of 15 packet in 1 box / 2 patch in 1 packet / 3 g in 1 patch of N-labs Arcticzen Pain Relief Knee, a human over the counter drug labeled by Nutriomo Labs Pte., Ltd. This patch is formulated for topical use and contains camphor (synthetic); 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 Nutriomo Labs Pte., Ltd on November 21, 2025. The current certification is valid through December 31, 2027.
How is this Nutriomo Labs Pte., Ltd product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71856035630. 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.