Foaming Mousse Anti-bacterial Hand Sanitizer Aerosol, Foam
NDC Package 56136-021-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Foaming Mousse Anti-bacterial Hand Sanitizer (alcohol) aerosols is avoid contact with eyes， if contact occurs rinse thoroughly with water. This formulation utilizes a aerosol, foam delivery system. Marketed by Ganzhou Olivee Cosmetic Co., Ltd., this product is identified by NDC 56136-021 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
56136-021-01
Package Description
50 mL in 1 BOTTLE
Product Code
56136-021
11-Digit Billing Format
56136002101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Foaming Mousse Anti-bacterial Hand Sanitizer Cherry Scented
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
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 62 mL/100mL
Usage Information
Avoid contact with eyes， if contact occurs rinse thoroughly with water.

Regulatory & Marketing

Labeler Name
Ganzhou Olivee Cosmetic Co., Ltd.
Product Type
Human Otc Drug
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
11-28-2018
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 56136-021-01 identifies a specific commercial package of 50 ml in 1 bottle of Foaming Mousse Anti-bacterial Hand Sanitizer Cherry Scented, a human over the counter drug labeled by Ganzhou Olivee Cosmetic Co., Ltd.. This aerosol, foam 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 Ganzhou Olivee Cosmetic Co., Ltd. on November 28, 2018. The current certification is valid through December 31, 2026.

How is this Ganzhou Olivee Cosmetic Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 56136002101. 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)
56136-021-01
11-Digit CMS (5-4-2)
56136-0021-01

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