Zkbb Wart Remover Liquid
NDC Package 87083-025-01

11-digit billing NDC: 87083002501
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Zkbb Wart Remover (salicylic acid) liquids is do not use on: moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face, irritated or infected skin. This formulation utilizes a liquid delivery system. Marketed by Guchutang Biotechnology (longyan) Co., Ltd, this product is identified by NDC 87083-025 and is authorized under FDA application M028.

Identification & Billing

NDC Package Code
87083-025-01
Package Description
40 mL in 1 BOTTLE
Product Code
87083-025
11-Digit Billing Format
87083002501

Clinical Specifications

Proprietary Name
Zkbb Wart Remover
Non-Proprietary Name
Salicylic Acid
Substance Name
Salicylic 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)
SALICYLIC ACID 5 g/100mL
Usage Information
Do not use on: moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face, irritated or infected skin. Ask a doctor before use if you have: diabetes, poor blood circulation, or immune system problems. When using this product: avoid contact with eyes; avoid contact with healthy surrounding skin. Stop use and ask a doctor if severe irritation occurs or the condition worsens. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Regulatory & Marketing

Labeler Name
Guchutang Biotechnology (longyan) Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M028
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-02-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 87083-025-01 identifies a specific commercial package of 40 ml in 1 bottle of Zkbb Wart Remover, a human over the counter drug labeled by Guchutang Biotechnology (longyan) Co., Ltd. This liquid is formulated for topical use and contains salicylic 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 Guchutang Biotechnology (longyan) Co., Ltd on November 02, 2026. The current certification is valid through December 31, 2027.

How is this Guchutang Biotechnology (longyan) Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87083002501. 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)
87083-025-01
11-Digit CMS (5-4-2)
87083-0025-01

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