NDC Package 75132-013-02 Foam Hand Sanitizer

View Billable Units, 11-Digit Format, RxNorm

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
75132-013-02
Package Description:
300 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Foam Hand Sanitizer
Usage Information:
Scope of application: Household and personal cleaning. Main Effect Effective inhibition of microorganisms category intestinal bacteria, pyogenic coccus.
11-Digit NDC Billing Format:
75132001302
Labeler Name:
Guangdong Kemei Pharmaceutical Technology Co., Ltd.
Sample Package:
No
Start Marketing Date:
04-12-2020
Listing Expiration Date:
12-31-2021
Exclude Flag:
I

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
75132-013-01236 mL in 1 BOTTLE
75132-013-03450 mL in 1 BOTTLE
75132-013-04500 mL in 1 BOTTLE
75132-013-051000 mL in 1 BOTTLE
75132-013-063785 mL in 1 BOTTLE
75132-013-075000 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 75132-013-02?

The NDC Packaged Code 75132-013-02 is assigned to a package of 300 ml in 1 bottle of Foam Hand Sanitizer, labeled by Guangdong Kemei Pharmaceutical Technology Co., Ltd.. The product's dosage form is and is administered via form.

Is NDC 75132-013 included in the NDC Directory?

No, Foam Hand Sanitizer with product code 75132-013 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Guangdong Kemei Pharmaceutical Technology Co., Ltd. on April 12, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 75132-013-02?

The 11-digit format is 75132001302. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-275132-013-025-4-275132-0013-02