Hand Sanitizer Liquid
NDC Package 87660-101-01

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

Package Information

Hand Sanitizer (alcohol) liquids is apply into hand and thoroughly spray on both hands, rub until dry. This formulation utilizes a liquid delivery system. Marketed by Guangdong Yanze Biotechnology Co., Ltd., this product is identified by NDC 87660-101 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
87660-101-01
Package Description
28 mL in 1 BOTTLE
Product Code
87660-101
11-Digit Billing Format
87660010101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Sanitizer
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
ALCOHOL 62 mL/100mL
Usage Information
Apply into hand and thoroughly spray on both hands, rub until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Regulatory & Marketing

Labeler Name
Guangdong Yanze Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-08-2026
Listing Expiration
12-31-2027
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 87660-101-01 identifies a specific commercial package of 28 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Guangdong Yanze Biotechnology Co., Ltd.. This liquid 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 Guangdong Yanze Biotechnology Co., Ltd. on May 08, 2026. The current certification is valid through December 31, 2027.

How is this Guangdong Yanze Biotechnology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87660010101. 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)
87660-101-01
11-Digit CMS (5-4-2)
87660-0101-01

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