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  5. NDC Package Code: 84844-007-01 Nekvnro Anti-itch Creme

NDC Package 84844-007-01 Nekvnro Anti-itch Creme

Anti-itch Creme Cream 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:
84844-007-01
Package Description:
30 g in 1 TUBE
Product Code:
84844-007
Proprietary Name:
Nekvnro Anti-itch Creme
Non-Proprietary Name:
Anti-itch Creme
Substance Name:
Bezlotoxumab
Usage Information:
Adults and children 12 years and older apply a fingertipamount (approximately 1-inch strip) to affected area not more than 3 to 4times daily.Clean nozzle of tube by wiping thoroughly before replacing cap.Keep cap tightly closed between uses. children under 12 years consult a doctor
11-Digit NDC Billing Format:
84844000701
Product Type:
Human Otc Drug
Labeler Name:
Guoyu Trading Co., Ltd.
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 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):
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):
BEZLOTOXUMAB 5 g/100g
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-31-2024
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 84844-007-01?

The NDC Packaged Code 84844-007-01 is assigned to a package of 30 g in 1 tube of Nekvnro Anti-itch Creme, a human over the counter drug labeled by Guoyu Trading Co., Ltd.. The product's dosage form is cream and is administered via topical form.

Is NDC 84844-007 included in the NDC Directory?

Yes, Nekvnro Anti-itch Creme with product code 84844-007 is active and included in the NDC Directory. The product was first marketed by Guoyu Trading Co., Ltd. on October 31, 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 84844-007-01?

The 11-digit format is 84844000701. 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
5-3-284844-007-015-4-284844-0007-01