Keke Hand Sanitizer Original 500ml Lt31042
NDC Package 54860-357-01

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.

Keke Hand Sanitizer Original 500ml Lt31042 is place enough product in your palm. Marketed by Shenzhen Lantern Scicence Co Ltd, this product is identified by NDC 54860-357 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
54860-357-01
Package Description
500 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
54860035701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Keke Hand Sanitizer Original 500ml Lt31042 01
Dosage Form
-
Usage Information
Place enough product in your palm. rub hands vigorously until dry.children under 6 years of age should be supervised when using this product.

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
04-18-2020
Listing Expiration
12-31-2022
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 54860-357-01 identifies a specific commercial package of 500 ml in 1 bottle, plastic of Keke Hand Sanitizer Original 500ml Lt31042 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 April 18, 2020. The current certification is valid through December 31, 2022.

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: 54860035701. 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)
54860-357-01
11-Digit CMS (5-4-2)
54860-0357-01

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