Alcohol Wipes Patch
NDC Package 77665-107-01

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

Alcohol Wipes patches is • storage: store at room temperature • dispensing: open protective seal, pull out wipe, reseal• use: wipe hands thoroughly For nail fungus, • disposal: do not fulsh. This formulation utilizes a patch delivery system. Marketed by Guangzhou Baihua Co., Ltd, this product is identified by NDC 77665-107 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
77665-107-01
Package Description
20 PATCH in 1 PACKAGE
Product Code
77665-107
11-Digit Billing Format
77665010701

Clinical Specifications

Proprietary Name
Alcohol Wipes
Non-Proprietary Name
Alcohol Wipes
Substance Name
Alcohol
Dosage Form
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
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 75 mL/1001
Usage Information
• storage: store at room temperature • dispensing: open protective seal, pull out wipe, reseal• use: wipe hands thoroughly For nail fungus, • disposal: do not fulsh

Regulatory & Marketing

Labeler Name
Guangzhou Baihua Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-24-2025
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (77665-107). Click a package code to view its specific billing and regulatory data.

77665-107-02
80 PATCH in 1 PACKAGE
77665-107-03
100 PATCH in 1 CANISTER

* 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 77665-107-01 identifies a specific commercial package of 20 patch in 1 package of Alcohol Wipes, a human over the counter drug labeled by Guangzhou Baihua Co., Ltd. This patch 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 Guangzhou Baihua Co., Ltd on November 24, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Baihua Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 77665010701. 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)
77665-107-01
11-Digit CMS (5-4-2)
77665-0107-01

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