Hand Sanitizer Liquid
NDC Package 87492-003-01

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

Package Information

Hand Sanitizer liquids is indications: This product is suitable for general skin disinfection and helps prevent the spread of diseases caused by bacteria. This formulation utilizes a liquid delivery system. Marketed by Shenzhen Yuehaotong Technology Co., Ltd, this product is identified by NDC 87492-003 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
87492-003-01
Package Description
1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE
Product Code
87492-003
11-Digit Billing Format
87492000301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Sanitizer
Non-Proprietary Name
Hand Sanitizer
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
Indications: This product is suitable for general skin disinfection and helps prevent the spread of diseases caused by bacteria. Directions: Before use, make sure your hands are dry. Apply an appropriate amount of this product to the palm of your hand (about one teaspoon or press the nozzle 2-3 times), rub your hands thoroughly until it evaporates completely, no need to rinse with water. Pay special attention to the cleaning of fingertips, around nails and thumbs. It is recommended to wait for hands to dry naturally after each use before touching food or other items. Precautions: Avoid contact with eyes. If contact occurs, rinse immediately with clean water. For external use only, avoid children using alone. This product is used as . Reduce or inhibit microbial growth, suitable for hand disinfection, helps reduce bacterial transmission

Regulatory & Marketing

Labeler Name
Shenzhen Yuehaotong Technology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-18-2026
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 87492-003-01 identifies a specific commercial package of 1 bottle in 1 box / 30 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Shenzhen Yuehaotong Technology 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 Shenzhen Yuehaotong Technology Co., Ltd on March 18, 2026. The current certification is valid through December 31, 2027.

How is this Shenzhen Yuehaotong Technology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87492000301. 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)
87492-003-01
11-Digit CMS (5-4-2)
87492-0003-01

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