Wart Remover Liquid
NDC Package 87298-043-01

11-digit billing NDC: 87298004301
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Wart Remover (salicylic acid) liquids is ●Wash the affected ared ●Soak the wart in warm water for 5 minutes and dry it thoroughly ●Anoly one drop at a time with the applicator to cover each wart completely alow to dry ●Use self-adhesive cushioning pads to cover the wart if desired Repeat this process once or twice daily as needed,for up to 12 weeks,until the wart is removed(Note:For external use,and can not be applied to healthy skin). This formulation utilizes a liquid delivery system. Marketed by Guangzhou Hechuang Commercial Service Co.,ltd., this product is identified by NDC 87298-043 and is authorized under FDA application M028.

Identification & Billing

NDC Package Code
87298-043-01
Package Description
30 g in 1 BOTTLE, PLASTIC
Product Code
87298-043
11-Digit Billing Format
87298004301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
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 15 g/100g
Usage Information
●Wash the affected ared ●Soak the wart in warm water for 5 minutes and dry it thoroughly ●Anoly one drop at a time with the applicator to cover each wart completely alow to dry ●Use self-adhesive cushioning pads to cover the wart if desired Repeat this process once or twice daily as needed,for up to 12 weeks,until the wart is removed(Note:For external use,and can not be applied to healthy skin)

Regulatory & Marketing

Labeler Name
Guangzhou Hechuang Commercial Service Co.,ltd.
Product Type
Human Otc Drug
FDA Application #
M028
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-23-2026
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 87298-043-01 identifies a specific commercial package of 30 g in 1 bottle, plastic of Wart Remover, a human over the counter drug labeled by Guangzhou Hechuang Commercial Service 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 Guangzhou Hechuang Commercial Service Co.,ltd. on June 23, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Hechuang Commercial Service Co.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87298004301. 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)
87298-043-01
11-Digit CMS (5-4-2)
87298-0043-01

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