Sani Luxe Hand Sanitizer With Alcohol Gel
NDC Package 71489-007-07

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Sani Luxe Hand Sanitizer With Alcohol (alcohol) gel is children under 6 years of age should be supervised when using this productPlace enough product in you palm to thoroughly cover your handsRub hands together briskly until dry. This formulation utilizes a gel delivery system. Marketed by Celeste Industries Corporation, this product is identified by NDC 71489-007 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
71489-007-07
Package Description
59 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
71489000707
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sani Luxe Hand Sanitizer With Alcohol
Non-Proprietary Name
Alcohol
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
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
Children under 6 years of age should be supervised when using this productPlace enough product in you palm to thoroughly cover your handsRub hands together briskly until dry

Regulatory & Marketing

Labeler Name
Celeste Industries Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-24-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71489-007). Click a package code to view its specific billing and regulatory data.

284 mL in 1 BOTTLE, PUMP
177 mL in 1 BOTTLE
59 mL in 1 BOTTLE, PUMP
237 mL in 1 BOTTLE, PUMP
355 mL in 1 BOTTLE, PUMP
3785 mL in 1 BOTTLE
177 mL in 1 BOTTLE, PUMP
237 mL in 1 BOTTLE
284 mL in 1 BOTTLE
355 mL in 1 BOTTLE
3785 mL in 1 BOTTLE, PUMP
946 mL in 1 BOTTLE, PUMP
946 mL in 1 BOTTLE
530 mL in 1 BOTTLE
530 mL in 1 BOTTLE, PUMP

* 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 71489-007-07 identifies a specific commercial package of 59 ml in 1 bottle of Sani Luxe Hand Sanitizer With Alcohol, a human over the counter drug labeled by Celeste Industries Corporation. This gel is formulated for cutaneous 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 Celeste Industries Corporation on January 24, 2019. The current certification is valid through December 31, 2026.

How is this Celeste Industries Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71489000707. 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)
71489-007-07
11-Digit CMS (5-4-2)
71489-0007-07

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