Instant Hand Sanitizer Liquid
NDC Package 75541-016-01

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

Package Information

Instant Hand Sanitizer liquids is directions ■ wet hands thoroughly with product and rub into skin until dry. This formulation utilizes a liquid delivery system. Marketed by Ningbo Meiteli Cosmetics Co., Ltd, this product is identified by NDC 75541-016 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
75541-016-01
Package Description
236 mL in 1 BOTTLE
Product Code
75541-016
11-Digit Billing Format
75541001601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Instant Hand Sanitizer
Non-Proprietary Name
Instant 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
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 70 mL/100mL
Usage Information
Directions ■ wet hands thoroughly with product and rub into skin until dry. ■Children under 6 years of age should be supervised by an adult when using.

Regulatory & Marketing

Labeler Name
Ningbo Meiteli Cosmetics Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-02-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (75541-016). Click a package code to view its specific billing and regulatory data.

75541-016-02
1000 mL in 1 BOTTLE

* 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 75541-016-01 identifies a specific commercial package of 236 ml in 1 bottle of Instant Hand Sanitizer, a human over the counter drug labeled by Ningbo Meiteli Cosmetics Co., Ltd. This liquid 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 Ningbo Meiteli Cosmetics Co., Ltd on February 02, 2026. The current certification is valid through December 31, 2027.

How is this Ningbo Meiteli Cosmetics Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75541001601. 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)
75541-016-01
11-Digit CMS (5-4-2)
75541-0016-01

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