NDC Package 65121-789-15 Zeta Clear Antifungal

Undecylenic Acid Solution 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:
65121-789-15
Package Description:
15 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Zeta Clear Antifungal
Non-Proprietary Name:
Undecylenic Acid
Substance Name:
Undecylenic Acid
Usage Information:
Clean and dry affected area with soap and water and dry thoroughly.Apply a thin layer to the affected area twice daily (morning and night) or as directed by physician.For athletes foot, pay special attention to the space between the toes, and wear well-fitting ventilated shoes and socks.For athlete's foot and ring worm.  If condition persists for longer, consult a physician.Intended for use by normally healthy adults only.  Persons under the age of 18, or those with highly sensitive or allergic skins hould use only as directed by physician.This product is not meant to be applied directly to the scalp or nails.
11-Digit NDC Billing Format:
65121078915
NDC to RxNorm Crosswalk:
  • RxCUI: 1251008 - undecylenic acid 10 % Topical Solution
  • RxCUI: 1251008 - undecylenic acid 100 MG/ML Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Pure Source, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-17-2017
    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.

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    Frequently Asked Questions

    What is NDC 65121-789-15?

    The NDC Packaged Code 65121-789-15 is assigned to a package of 15 ml in 1 bottle of Zeta Clear Antifungal, a human over the counter drug labeled by Pure Source, Llc. The product's dosage form is solution and is administered via topical form.

    Is NDC 65121-789 included in the NDC Directory?

    Yes, Zeta Clear Antifungal with product code 65121-789 is active and included in the NDC Directory. The product was first marketed by Pure Source, Llc on February 17, 2017 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 65121-789-15?

    The 11-digit format is 65121078915. 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
    5-3-265121-789-155-4-265121-0789-15