Sodoer Hand Mask
NDC Package 84775-043-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Sodoer Hand Mask is how to use: 1.Clean and dry your feet, then remove the productfrom the bag. Marketed by Shenzhen Fusian Technology Co Ltd, this product is identified by NDC 84775-043 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
84775-043-01
Package Description
35 g in 1 BLISTER PACK
Product Code
11-Digit Billing Format
84775004301

Clinical Specifications

Proprietary Name
Sodoer Hand Mask
Dosage Form
-
Usage Information
How to use: 1.Clean and dry your feet, then remove the productfrom the bag. 2.Put on the foot mask, gently press the outer layer ofthe mask so that the foot is in close contact with themask.3.After about 20-40 minutes, you can take off the footmask, wash with water, and then use foot cream totake care of your feet.4.Depending on the condition of the feet to do regularcare.

Regulatory & Marketing

Labeler Name
Shenzhen Fusian Technology Co Ltd
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-18-2024
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 84775-043-01 identifies a specific commercial package of 35 g in 1 blister pack of Sodoer Hand Mask, labeled by Shenzhen Fusian Technology 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 Shenzhen Fusian Technology Co Ltd on November 18, 2024. The current certification is valid through December 31, 2025.

How is this Shenzhen Fusian Technology Co Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84775004301. 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)
84775-043-01
11-Digit CMS (5-4-2)
84775-0043-01

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