Aiilo Nail Fungus Treatment Liquid
NDC Package 87204-190-01

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

Package Information

Aiilo Nail Fungus Treatment (undecylenic acid 25%) liquids is including discoloration, thickening, splitting, crumbling, and brittleness.Directions: 1 Apply the product twice a day, in the morning and at night 2. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Huixue Biotechnology Co., Ltd., this product is identified by NDC 87204-190 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
87204-190-01
Package Description
30 mL in 1 BOTTLE, PLASTIC
Product Code
87204-190
11-Digit Billing Format
87204019001

Clinical Specifications

Proprietary Name
Aiilo Nail Fungus Treatment
Non-Proprietary Name
Undecylenic Acid 25%
Substance Name
Undecylenic Acid
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)
UNDECYLENIC ACID .25 mg/30mL
Usage Information
Including discoloration, thickening, splitting, crumbling, and brittleness.Directions: 1 Apply the product twice a day, in the morning and at night 2. For initial use, soak the affected nail in warm water to soften it, Gently file the nail to make it thinner and remove debris, being cautious not to harm the nail bed, For best results file nails every 2-3 days 3. Hold the bottle at an angle and apply 2-3 drops of the solution evenly to the affected area 4 Visible improvement may be seen in as little as 7 days, Continue regular use to help prevent fungus regrowth.

Regulatory & Marketing

Labeler Name
Guangzhou Huixue Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-04-2026
End Marketing Date
07-10-2027
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 87204-190-01 identifies a specific commercial package of 30 ml in 1 bottle, plastic of Aiilo Nail Fungus Treatment, a human over the counter drug labeled by Guangzhou Huixue Biotechnology Co., Ltd.. This liquid is formulated for topical use and contains undecylenic acid 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 Huixue Biotechnology Co., Ltd. on July 04, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87204019001. 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)
87204-190-01
11-Digit CMS (5-4-2)
87204-0190-01

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