NDC Package 84010-192-01 Gaayou Numbing

Dibucaine Hydrochloride 0.5% Numbing Cream Topical - View Billable Units, 11-Digit Format, RxNorm

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:
84010-192-01
Package Description:
50 g in 1 BOTTLE
Product Code:
Proprietary Name:
Gaayou Numbing
Non-Proprietary Name:
Dibucaine Hydrochloride 0.5% Numbing
Substance Name:
Dibucaine Hydrochloride
Usage Information:
Before applying the numbing cream,make sure to wash your hands thoroughly and put on disposable procedure gloves. Clean the area of the body receivina the procedure,Dry completely. Apply a generous amount of numbing cream to the cleaned area and rub it in thoroughly in a circlar motion for 30 to 60 seconds,Then. cover with plastic wrap. Leave the cream and wrap in place for 30 to 45 minutes,Wipe away the cream and thoroughly clean the area to prepare for the upcoming procedure.
11-Digit NDC Billing Format:
84010019201
Product Type:
Human Otc Drug
Labeler Name:
Jiangxi Hemei Pharmaceutical 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.
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
09-29-2025
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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Frequently Asked Questions

What is NDC 84010-192-01?

The NDC Packaged Code 84010-192-01 is assigned to a package of 50 g in 1 bottle of Gaayou Numbing, a human over the counter drug labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. The product's dosage form is cream and is administered via topical form.

Is NDC 84010-192 included in the NDC Directory?

Yes, Gaayou Numbing with product code 84010-192 is active and included in the NDC Directory. The product was first marketed by Jiangxi Hemei Pharmaceutical Co., Ltd on September 29, 2025 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 84010-192-01?

The 11-digit format is 84010019201. 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
5-3-284010-192-015-4-284010-0192-01