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  5. NDC Package Code: 84778-027-01 Sheetsmartwartremoverointment

NDC Package 84778-027-01 Sheetsmartwartremoverointment

Ointment Cutaneous - 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:
84778-027-01
Package Description:
20 g in 1 BOX
Product Code:
84778-027
Proprietary Name:
Sheetsmartwartremoverointment
Non-Proprietary Name:
Sheetsmart Wart Remover Ointment
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:
84778002701
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Yixin Cross-border E-commerce Co., Ltd.
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Cutaneous - Administration to the skin.
Active Ingredient(s):
SALICYLIC ACID 1 g/20g
Sample Package:
No
FDA Application Number:
M028
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-25-2024
Listing Expiration Date:
12-31-2025
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 84778-027-01?

The NDC Packaged Code 84778-027-01 is assigned to a package of 20 g in 1 box of Sheetsmartwartremoverointment, a human over the counter drug labeled by Guangzhou Yixin Cross-border E-commerce Co., Ltd.. The product's dosage form is ointment and is administered via cutaneous form.

Is NDC 84778-027 included in the NDC Directory?

Yes, Sheetsmartwartremoverointment with product code 84778-027 is active and included in the NDC Directory. The product was first marketed by Guangzhou Yixin Cross-border E-commerce Co., Ltd. on October 25, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84778-027-01?

The 11-digit format is 84778002701. 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
5-3-284778-027-015-4-284778-0027-01