NDC Package 80569-084-15 Flush Maximum Strength Antifungal Formula

Undecylenic Acid Liquid 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:
80569-084-15
Package Description:
15 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Flush Maximum Strength Antifungal Formula
Non-Proprietary Name:
Undecylenic Acid
Substance Name:
Undecylenic Acid
Usage Information:
Clean and dry affected area with soap and water and dry throughly.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 ringworm. If Conditions persists for longer, consult a physician.Intended for use typically by healthy adults only. Persons under the age of 18, or those with highly sensitive or allergic skin should 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:
80569008415
NDC to RxNorm Crosswalk:
  • RxCUI: 998329 - undecylenic acid 25 % Topical Solution
  • RxCUI: 998329 - undecylenic acid 250 MG/ML Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Triple Point Group, Llc
    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(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:
    09-17-2020
    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 80569-084-15?

    The NDC Packaged Code 80569-084-15 is assigned to a package of 15 ml in 1 bottle, glass of Flush Maximum Strength Antifungal Formula, a human over the counter drug labeled by Triple Point Group, Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 80569-084 included in the NDC Directory?

    Yes, Flush Maximum Strength Antifungal Formula with product code 80569-084 is active and included in the NDC Directory. The product was first marketed by Triple Point Group, Llc on September 17, 2020 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 80569-084-15?

    The 11-digit format is 80569008415. 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
    5-3-280569-084-155-4-280569-0084-15