Skin Tag Remover Liquid
NDC Package 84019-036-01

11-digit billing NDC: 84019003601

Package Information

Skin Tag Remover (salicylic acid) liquids is sTEP 1:Wash the affected area wtih warm water、thendry it.STEP 2:Apply this product on the part oftheskinwhere there is growth.Use a cottonswab.STEP 3:Use twice daily、 once in the morning andonce in the evening.Stop using the product when the carcass turns white and the affected area hasvisibly healed.Healingshould be complete within 20 days upon use. This formulation utilizes a liquid delivery system. Marketed by Shengnan (guangzhou) Cosmetics Co., Ltd, this product is identified by NDC 84019-036 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
84019-036-01
Package Description
20 g in 1 BOTTLE
Product Code
11-Digit Billing Format
84019003601

Clinical Specifications

Proprietary Name
Skin Tag 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
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
STEP 1:Wash the affected area wtih warm water、thendry it.STEP 2:Apply this product on the part oftheskinwhere there is growth.Use a cottonswab.STEP 3:Use twice daily、 once in the morning andonce in the evening.Stop using the product when the carcass turns white and the affected area hasvisibly healed.Healingshould be complete within 20 days upon use.

Regulatory & Marketing

Labeler Name
Shengnan (guangzhou) Cosmetics Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-16-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 84019-036-01 identifies a specific commercial package of 20 g in 1 bottle of Skin Tag Remover, a human over the counter drug labeled by Shengnan (guangzhou) Cosmetics Co., Ltd. This liquid is formulated for cutaneous 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 Shengnan (guangzhou) Cosmetics Co., Ltd on September 16, 2025. The current certification is valid through December 31, 2026.

How is this Shengnan (guangzhou) Cosmetics Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84019003601. 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)
84019-036-01
11-Digit CMS (5-4-2)
84019-0036-01

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