Mellow Hand Sanitizer 59ml Ml316
NDC Package 54860-252-01

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.

Mellow Hand Sanitizer 59ml Ml316 is wet hands thoroughly with product and rub until dry without wipingFor children under 6, use only under adult supervision.Not recommended for infants. Marketed by Shenzhen Lantern Scicence Co.,ltd., this product is identified by NDC 54860-252 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
54860-252-01
Package Description
59 mL in 1 TUBE
Product Code
11-Digit Billing Format
54860025201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Mellow Hand Sanitizer 59ml Ml316 01
Dosage Form
-
Usage Information
Wet hands thoroughly with product and rub until dry without wipingFor children under 6, use only under adult supervision.Not recommended for infants.

Regulatory & Marketing

Labeler Name
Shenzhen Lantern Scicence Co.,ltd.
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
05-09-2020
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
Yes

Hierarchy Structure

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 54860-252-01 identifies a specific commercial package of 59 ml in 1 tube of Mellow Hand Sanitizer 59ml Ml316 01, labeled by Shenzhen Lantern Scicence 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 Lantern Scicence Co.,ltd. on May 09, 2020. The current certification is valid through December 31, 2021.

How is this Shenzhen Lantern Scicence Co.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54860025201. 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)
54860-252-01
11-Digit CMS (5-4-2)
54860-0252-01

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