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  5. NDC Package Code: 74458-276-01 Melao Callus Remover

NDC Package 74458-276-01 Melao Callus Remover

Urea 10% Pumice Extract 5% Gel 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:
74458-276-01
Package Description:
250 mL in 1 BOTTLE, PLASTIC
Product Code:
74458-276
Proprietary Name:
Melao Callus Remover
Non-Proprietary Name:
Urea 10% Pumice Extract 5%
Substance Name:
Pumice; Urea
Usage Information:
Put Gloves on. 1. Soak feet in warm water until prune-like. 2. Pre scrub with pumice stone or foot rasp.(Optional but recommended) 3. Towel dry one foot, apply callus remover to hard and dry callused areas(avoid soft skin), and let sit for 5-10 minutes. 4. You can scrub with pumice or rasp while callus remover is on.(Optional but recommended) 5. Rinse foot and use pumice stone or rasp to remove extra residue of callus remover and dead skin. 6.Repeat above process for other foot. Note: Some peoples calluses maybe worse than others,so repeat callus remover process as necessary.
11-Digit NDC Billing Format:
74458027601
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Yilong Cosmetics Co., Ltd
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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):
Sample Package:
No
FDA Application Number:
M030
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-03-2024
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 74458-276-01?

The NDC Packaged Code 74458-276-01 is assigned to a package of 250 ml in 1 bottle, plastic of Melao Callus Remover, a human over the counter drug labeled by Guangzhou Yilong Cosmetics Co., Ltd. The product's dosage form is gel and is administered via topical form.

Is NDC 74458-276 included in the NDC Directory?

Yes, Melao Callus Remover with product code 74458-276 is active and included in the NDC Directory. The product was first marketed by Guangzhou Yilong Cosmetics Co., Ltd on October 03, 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 74458-276-01?

The 11-digit format is 74458027601. 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
5-3-274458-276-015-4-274458-0276-01