Lanozem Hemorrhoidal Ointment
NDC Package 84483-0010-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Lanozem Hemorrhoidal (menthol, petrolatum) ointment is adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. This formulation utilizes a ointment delivery system. Marketed by Sod-e Biotech Ltd, this product is identified by NDC 84483-0010 and is authorized under FDA application M015.

Identification & Billing

NDC Package Code
84483-0010-1
Package Description
10 TUBE in 1 CARTON / 3 g in 1 TUBE
Product Code
84483-0010
11-Digit Billing Format
84483001001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Lanozem Hemorrhoidal
Non-Proprietary Name
Menthol, Petrolatum
Substance Name
Menthol; Petrolatum
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
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)
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

Regulatory & Marketing

Labeler Name
Sod-e Biotech Ltd
Product Type
Human Otc Drug
FDA Application #
M015
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-07-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 84483-0010-1 identifies a specific commercial 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. This ointment is formulated for topical use and contains menthol; petrolatum as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Sod-e Biotech Ltd on May 07, 2025. The current certification is valid through December 31, 2026.

How is this Sod-e Biotech Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84483001001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
84483-0010-1
11-Digit CMS (5-4-2)
84483-0010-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.