1. Home
  2. Labeler Index
  3. Industria Quimico Farmaceutica Sigma Corp. S.r.l.
  4. 84831-096
  5. NDC Package Code: 84831-096-01 Coca Lief

NDC Package 84831-096-01 Coca Lief

Menthol,Methylsalicylate Gel 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:
84831-096-01
Package Description:
100000 mg in 1 TUBE
Product Code:
84831-096
Proprietary Name:
Coca Lief
Non-Proprietary Name:
Menthol, Methylsalicylate
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
For External Use Only
11-Digit NDC Billing Format:
84831009601
Product Type:
Human Otc Drug
Labeler Name:
Industria Quimico Farmaceutica Sigma Corp. S.r.l.
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
01-20-2025
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 84831-096-01?

The NDC Packaged Code 84831-096-01 is assigned to a package of 100000 mg in 1 tube of Coca Lief, a human over the counter drug labeled by Industria Quimico Farmaceutica Sigma Corp. S.r.l.. The product's dosage form is gel and is administered via topical form.

Is NDC 84831-096 included in the NDC Directory?

Yes, Coca Lief with product code 84831-096 is active and included in the NDC Directory. The product was first marketed by Industria Quimico Farmaceutica Sigma Corp. S.r.l. on January 20, 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 84831-096-01?

The 11-digit format is 84831009601. 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
5-3-284831-096-015-4-284831-0096-01