Sinsinpas Pain Relieving Patch
NDC Package 55264-101-03

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Sinsinpas Pain Relieving Patch is adults and children 12 years of age and over:Clean and dry affected areaRemove patch from filmApply to affected area no more than 3 to 4 times daily for 7 daysRemove patch from skin after at most 8 hours’ applicationChildren undress 12 years of age: consult a doctor. Marketed by Sinsin Pharmaceutical Co., Ltd., this product is identified by NDC 55264-101 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
55264-101-03
Package Description
2 POUCH in 1 PACKAGE / 20 PATCH in 1 POUCH (55264-101-02) / 459.93 g in 1 PATCH (55264-101-01)
Product Code
55264-101
11-Digit Billing Format
55264010103
RxNorm Crosswalk
  • RxCUI: 2102942 - camphor 1.21 % / L-menthol 5.54 % / methyl salicylate 6.11 % Medicated Patch
  • RxCUI: 2102942 - camphor 5560 MG / levomenthol 2550 MG / methyl salicylate 28100 MG Medicated Patch

Clinical Specifications

Proprietary Name
Sinsinpas Pain Relieving Patch
Dosage Form
-
Usage Information
Adults and children 12 years of age and over:Clean and dry affected areaRemove patch from filmApply to affected area no more than 3 to 4 times daily for 7 daysRemove patch from skin after at most 8 hours’ applicationChildren undress 12 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Sinsin Pharmaceutical Co., Ltd.
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2017
Listing Expiration
12-31-2025
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55264-101-03 identifies a specific commercial package of 2 pouch in 1 package / 20 patch in 1 pouch (55264-101-02) / 459.93 g in 1 patch (55264-101-01) of Sinsinpas Pain Relieving Patch, labeled by Sinsin Pharmaceutical Co., Ltd.. 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 Sinsin Pharmaceutical Co., Ltd. on May 01, 2017. The current certification is valid through December 31, 2025.

How is this Sinsin Pharmaceutical Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55264010103. 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:

10-Digit Format (5-3-2)
55264-101-03
11-Digit CMS (5-4-2)
55264-0101-03

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.