Hand Sanitizer Gel
NDC Package 79805-001-07

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

Hand Sanitizer gel is wet hands thoroughly with product and allow to dry wthout wiping. This formulation utilizes a gel delivery system. Marketed by Juxin (jiangsu) New Material Packaging Co., Ltd., this product is identified by NDC 79805-001.

Identification & Billing

NDC Package Code
79805-001-07
Package Description
100 mL in 1 BOTTLE
Product Code
79805-001
11-Digit Billing Format
79805000107
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Sanitizer
Non-Proprietary Name
Hand Sanitizer
Substance Name
Alcohol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALCOHOL 68 mL/100mL
Usage Information
Wet hands thoroughly with product and allow to dry wthout wiping. For children under 6, use only under adult supervision Not recommended for infants

Regulatory & Marketing

Labeler Name
Juxin (jiangsu) New Material Packaging Co., Ltd.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
03-30-2020
Listing Expiration
12-31-2026
Exclude Flag
N
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 (79805-001). Click a package code to view its specific billing and regulatory data.

79805-001-01
60 mL in 1 BOTTLE
79805-001-02
120 mL in 1 BOTTLE
79805-001-03
300 mL in 1 BOTTLE
79805-001-04
500 mL in 1 BOTTLE
79805-001-05
3800 mL in 1 BOTTLE
79805-001-06
90 mL in 1 BOTTLE
79805-001-08
750 mL in 1 BOTTLE
79805-001-09
1000 mL in 1 BOTTLE
79805-001-10
18 mL in 1 BOTTLE
79805-001-11
250 mL in 1 BOTTLE
79805-001-12
2000 mL in 1 BOTTLE

* 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 79805-001-07 identifies a specific commercial package of 100 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Juxin (jiangsu) New Material Packaging Co., Ltd.. This gel is formulated for topical use and contains alcohol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Juxin (jiangsu) New Material Packaging Co., Ltd. on March 30, 2020. The current certification is valid through December 31, 2026.

How is this Juxin (jiangsu) New Material Packaging Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79805000107. 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)
79805-001-07
11-Digit CMS (5-4-2)
79805-0001-07

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