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  5. NDC Package Code: 28691-0400-2 Wart Remover

NDC Package 28691-0400-2 Wart Remover

Salicylic Acid Plaster Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
28691-0400-2
Package Description:
10 PLASTER in 1 BOX
Product Code:
28691-0400
Proprietary Name:
Wart Remover
Non-Proprietary Name:
Salicylic Acid
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:
28691040002
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Pharmaplast Sae
Dosage Form:
Plaster - Substance intended for external application made of such materials and of such consistency as to adhere to the skin and attach to a dressing; plasters are intended to afford protection and support and/or to furnish an occlusion and macerating action and to bring medication into close contact with the skin.
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 .4 g/1
Sample Package:
No
FDA Application Number:
M030
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-07-2016
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
28691-0400-120 PLASTER in 1 BOX

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 28691-0400-2?

The NDC Packaged Code 28691-0400-2 is assigned to a package of 10 plaster in 1 box of Wart Remover, a human over the counter drug labeled by Pharmaplast Sae. The product's dosage form is plaster and is administered via topical form.

Is NDC 28691-0400 included in the NDC Directory?

Yes, Wart Remover with product code 28691-0400 is active and included in the NDC Directory. The product was first marketed by Pharmaplast Sae on October 07, 2016 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 28691-0400-2?

The 11-digit format is 28691040002. 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 5-4-1 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
5-4-128691-0400-25-4-228691-0400-02