NDC Package 50066-010-09 Nikzon Hemorrhoidal

Glycerin,Petrolatum,Phenylephrine Hydrochloride,And Pramoxine Hydrochloride 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:
50066-010-09
Package Description:
1 TUBE in 1 CARTON / 25.5 g in 1 TUBE
Product Code:
Proprietary Name:
Nikzon Hemorrhoidal
Non-Proprietary Name:
Glycerin, Petrolatum, Phenylephrine Hydrochloride, And Pramoxine Hydrochloride
Substance Name:
Glycerin; Petrolatum; Phenylephrine Hydrochloride; Pramoxine Hydrochloride
Usage Information:
Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing pad. Gently dry by patting or blotting with a tissue or a soft cloth before applying creamapply externally to the affected area up to 4 times daily or after each bowel movementchildren under 12 years old: consult a physician
11-Digit NDC Billing Format:
50066001009
NDC to RxNorm Crosswalk:
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine HCl 0.25 % / pramoxine HCl 1 % / white petrolatum 15 % Rectal Cream
  • RxCUI: 1293649 - glycerin 144 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 15 % Rectal Cream
Product Type:
Human Otc Drug
Labeler Name:
Genomma Lab Usa
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:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-07-2025
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50066-010-09?

The NDC Packaged Code 50066-010-09 is assigned to a package of 1 tube in 1 carton / 25.5 g in 1 tube of Nikzon Hemorrhoidal, a human over the counter drug labeled by Genomma Lab Usa. The product's dosage form is cream and is administered via topical form.

Is NDC 50066-010 included in the NDC Directory?

Yes, Nikzon Hemorrhoidal with product code 50066-010 is active and included in the NDC Directory. The product was first marketed by Genomma Lab Usa on July 07, 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 50066-010-09?

The 11-digit format is 50066001009. 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
5-3-250066-010-095-4-250066-0010-09