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  5. NDC Package Code: 85834-002-01 Wart Remover

NDC Package 85834-002-01 Wart Remover

Salicylic Acid 17% Wart Remover Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
85834-002-01
Package Description:
30 mL in 1 BOTTLE
Product Code:
85834-002
Proprietary Name:
Wart Remover
Non-Proprietary Name:
Salicylic Acid 17% Wart Remover
Substance Name:
Salicylic Acid
Usage Information:
This medication is used on the skin to treat common skin and foot (plantar) warts. Salicylic acid helps cause the wart to gradually peel off. This medication is also used to help remove corns and calluses. This product should not be used on the face or on moles, birthmarks, warts with hair growing from them, or genital/anal warts. Salicylic acid is a keratolytic. It belongs to the same class of drugs as aspirin (salicylates). It works by increasing the amount of moisture in the skin and dissolving the substance that causes the skin cells to stick together. This makes it easier to shed the skin cells. Warts are caused by a virus. Salicylic acid does not affect the virus.
11-Digit NDC Billing Format:
85834000201
Product Type:
Human Otc Drug
Labeler Name:
Shenzhen Bullfighting Trading Co., Ltd.
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(s):
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 17 g/100mL
Sample Package:
No
FDA Application Number:
M028
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
06-30-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 85834-002-01?

The NDC Packaged Code 85834-002-01 is assigned to a package of 30 ml in 1 bottle of Wart Remover, a human over the counter drug labeled by Shenzhen Bullfighting Trading Co., Ltd.. The product's dosage form is liquid and is administered via topical form.

Is NDC 85834-002 included in the NDC Directory?

Yes, Wart Remover with product code 85834-002 is active and included in the NDC Directory. The product was first marketed by Shenzhen Bullfighting Trading Co., Ltd. on June 30, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85834-002-01?

The 11-digit format is 85834000201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-285834-002-015-4-285834-0002-01