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  5. NDC Package Code: 84483-0010-1 Lanozem Hemorrhoidal

NDC Package 84483-0010-1 Lanozem Hemorrhoidal

Menthol,Petrolatum Ointment 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:
84483-0010-1
Package Description:
10 TUBE in 1 CARTON / 3 g in 1 TUBE
Product Code:
84483-0010
Proprietary Name:
Lanozem Hemorrhoidal
Non-Proprietary Name:
Menthol, Petrolatum
Substance Name:
Menthol; Petrolatum
Usage Information:
Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by blotting or patting with a tissue or a soft cloth before applying ointment.Apply to the affected area up to 6 times daily, especially at night, in the morning or after ' each bowel movement.EXTERNAL USE: Apply to external anal area.INTRARECTAL USE: Lubricate applicator well with Lonazem ointment, then gently insert applicator into the rectum.Children under 12 years of age: consult a doctor
11-Digit NDC Billing Format:
84483001001
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Sod-e Biotech 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):
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:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-07-2025
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 84483-0010-1?

The NDC Packaged Code 84483-0010-1 is assigned to a package of 10 tube in 1 carton / 3 g in 1 tube of Lanozem Hemorrhoidal, a human over the counter drug labeled by Sod-e Biotech Ltd. The product's dosage form is ointment and is administered via topical form.

Is NDC 84483-0010 included in the NDC Directory?

Yes, Lanozem Hemorrhoidal with product code 84483-0010 is active and included in the NDC Directory. The product was first marketed by Sod-e Biotech Ltd on May 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 84483-0010-1?

The 11-digit format is 84483001001. 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 5-4-1 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
5-4-184483-0010-15-4-284483-0010-01