NDC Package 72751-0301-1 Zilactin Early Relief Cold Sore

Benzyl Alcohol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

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:
72751-0301-1
Package Description:
1 TUBE in 1 CARTON / 7.1 g in 1 TUBE
Product Code:
Proprietary Name:
Zilactin Early Relief Cold Sore
Non-Proprietary Name:
Benzyl Alcohol
Substance Name:
Benzyl Alcohol
Usage Information:
Adults and children 2 years and older dry affected area. Apply with cotton swab or clean finger up to 4 times daily. Allow to dry 30-60 seconds. children under 12 years adult supervision should be given in the use of this product children under 2 years do not use, consult a physician or dentist
11-Digit NDC Billing Format:
72751030101
NDC to RxNorm Crosswalk:
  • RxCUI: 581456 - benzyl alcohol 10 % Oral Gel
  • RxCUI: 581456 - benzyl alcohol 0.1 ML/ML Oral Gel
  • RxCUI: 581456 - benzyl alcohol 10 % Mucous Membrane Topical Gel
  • RxCUI: 866357 - zilactin Early Relief Cold Sore 10 % Oral Gel
  • RxCUI: 866357 - benzyl alcohol 0.1 ML/ML Oral Gel [Zilactin Cold Sore]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Applied Laboratories, Inc.
    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
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-30-2005
    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 72751-0301-1?

    The NDC Packaged Code 72751-0301-1 is assigned to a package of 1 tube in 1 carton / 7.1 g in 1 tube of Zilactin Early Relief Cold Sore, a human over the counter drug labeled by Applied Laboratories, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 72751-0301 included in the NDC Directory?

    Yes, Zilactin Early Relief Cold Sore with product code 72751-0301 is active and included in the NDC Directory. The product was first marketed by Applied Laboratories, Inc. on June 30, 2005 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 72751-0301-1?

    The 11-digit format is 72751030101. 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
    5-4-172751-0301-15-4-272751-0301-01