Hand Sanitizer Spray
NDC Package 87858-001-01

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

Package Information

Hand Sanitizer (ethyl alcohol) sprays is · Spray a small amount in your palm and briskly rub hands together until dry. This formulation utilizes a spray delivery system. Marketed by Nantong Haiyiwei Textile Co., Ltd., this product is identified by NDC 87858-001 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
87858-001-01
Package Description
35 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
87858000101

Clinical Specifications

Proprietary Name
Hand Sanitizer
Non-Proprietary Name
Ethyl Alcohol
Substance Name
Alcohol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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)
Usage Information
· Spray a small amount in your palm and briskly rub hands together until dry. · Supervise children under 6 years of age when using this product to avoid swallowing.

Regulatory & Marketing

Labeler Name
Nantong Haiyiwei Textile Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-16-2026
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 87858-001-01 identifies a specific commercial package of 35 ml in 1 bottle of Hand Sanitizer, a human over the counter drug labeled by Nantong Haiyiwei Textile Co., Ltd.. This spray 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 Nantong Haiyiwei Textile Co., Ltd. on July 16, 2026. The current certification is valid through December 31, 2027.

How is this Nantong Haiyiwei Textile Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87858000101. 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)
87858-001-01
11-Digit CMS (5-4-2)
87858-0001-01

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