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  5. NDC Package Code: 67194-017-01 Liprotek

NDC Package 67194-017-01 Liprotek

Petrolatum,Lidocaine 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:
67194-017-01
Package Description:
4 g in 1 JAR
Product Code:
67194-017
Proprietary Name:
Liprotek
Non-Proprietary Name:
Petrolatum, Lidocaine
Substance Name:
Lidocaine; Petrolatum
Usage Information:
TEMPORARY RELIEF OF PAIN and/or ITCHING FROM FEVER BLISTERS and COLD SORES TEMPORARY RELIEF OF PAIN AND/OR ITCHING FROM FEVER BLISTERS AND COLD SORESThis product is used as . Skin ProtectantExternal or Topical Analgesic
11-Digit NDC Billing Format:
67194001701
Product Type:
Human Otc Drug
Labeler Name:
Unit Dose, 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):
  • LIDOCAINE 6 mg/g
  • PETROLATUM 610 mg/g
    • Pharmacologic Class(es):
  • Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
  • Amides - [CS]
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
  • Local Anesthesia - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-21-2016
    Listing Expiration Date:
    12-31-2024
    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 67194-017-01?

    The NDC Packaged Code 67194-017-01 is assigned to a package of 4 g in 1 jar of Liprotek, a human over the counter drug labeled by Unit Dose, Ltd.. The product's dosage form is ointment and is administered via topical form.

    Is NDC 67194-017 included in the NDC Directory?

    Yes, Liprotek with product code 67194-017 is active and included in the NDC Directory. The product was first marketed by Unit Dose, Ltd. on January 21, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67194-017-01?

    The 11-digit format is 67194001701. 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
    5-3-267194-017-015-4-267194-0017-01