Medi Fect Liquid
NDC Package 12745-177-01

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

Package Information

Medi Fect (ethyl alcohol) liquids is indications for use: For hospital and professional use only.  Medi-Fect is intended to be used as a hand-wash to reduce bacteria that can potentially cause disease. This formulation utilizes a liquid delivery system. Marketed by Medical Chemical Corporation, this product is identified by NDC 12745-177 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
12745-177-01
Package Description
118 mL in 1 BOTTLE, PLASTIC
Product Code
12745-177
11-Digit Billing Format
12745017701

Clinical Specifications

Proprietary Name
Medi Fect Antiseptic Hand Wash
Non-Proprietary Name
Ethyl Alcohol
Substance Name
Alcohol; Diazolidinyl Urea
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
Pharmacologic Class
Usage Information
Indications for use: For hospital and professional use only.  Medi-Fect is intended to be used as a hand-wash to reduce bacteria that can potentially cause disease. Recommended for repeated use.

Regulatory & Marketing

Labeler Name
Medical Chemical Corporation
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-14-2001
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (12745-177). Click a package code to view its specific billing and regulatory data.

12745-177-02
473 mL in 1 BOTTLE, PLASTIC
12745-177-03
3785 mL in 1 BOTTLE, PLASTIC
12745-177-04
18927 mL in 1 BOTTLE, PLASTIC
12745-177-05
59 mL in 1 BOTTLE, PLASTIC
12745-177-06
237 mL in 1 BOTTLE, PLASTIC
12745-177-07
946 mL in 1 BOTTLE, PLASTIC
12745-177-08
208198 mL in 1 DRUM

* 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 12745-177-01 identifies a specific commercial package of 118 ml in 1 bottle, plastic of Medi Fect Antiseptic Hand Wash, a human over the counter drug labeled by Medical Chemical Corporation. This liquid is formulated for topical use and contains alcohol; diazolidinyl urea 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 Medical Chemical Corporation on May 14, 2001. The current certification is valid through December 31, 2026.

How is this Medical Chemical Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 12745017701. 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 (5-3-2)
12745-177-01
11-Digit CMS (5-4-2)
12745-0177-01

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