Hand Sanitizer
NDC Package 50260-200-10

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

Package Information

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

Hand Sanitizer is wet hands thoroughly with product and rub hands together until dry. Marketed by Fercy Personal Care Products Co Limited, this product is identified by NDC 50260-200 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
50260-200-10
Package Description
240 mL in 1 BOTTLE, PLASTIC
Product Code
50260-200
11-Digit Billing Format
50260020010
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Sanitizer
Dosage Form
-
Usage Information
Wet hands thoroughly with product and rub hands together until dry. No need to wash or rinse your handsor use towels.Supervise children under 6 years of age.

Regulatory & Marketing

Labeler Name
Fercy Personal Care Products Co Limited
FDA Application #
part348
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-01-2010
Listing Expiration
12-31-2017
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (50260-200). Click a package code to view its specific billing and regulatory data.

50260-200-01
5 mL in 1 BOTTLE, PLASTIC
50260-200-02
8 mL in 1 BOTTLE, PLASTIC
50260-200-03
10 mL in 1 BOTTLE, PLASTIC
50260-200-04
20 mL in 1 BOTTLE, PLASTIC
50260-200-05
30 mL in 1 BOTTLE, PLASTIC
50260-200-06
50 mL in 1 BOTTLE, PLASTIC
50260-200-07
60 mL in 1 BOTTLE, PLASTIC
50260-200-08
100 mL in 1 BOTTLE, PLASTIC
50260-200-09
120 mL in 1 BOTTLE, PLASTIC
50260-200-11
360 mL in 1 BOTTLE, PLASTIC
50260-200-12
500 mL in 1 BOTTLE, PLASTIC
50260-200-13
1000 mL in 1 BOTTLE, PLASTIC

* 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 50260-200-10 identifies a specific commercial package of 240 ml in 1 bottle, plastic of Hand Sanitizer, labeled by Fercy Personal Care Products Co Limited. 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 Fercy Personal Care Products Co Limited on February 01, 2010. The current certification is valid through December 31, 2017.

How is this Fercy Personal Care Products Co Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50260020010. 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)
50260-200-10
11-Digit CMS (5-4-2)
50260-0200-10

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