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  5. NDC Package Code: 80569-101-15 Crystal Flush Maximum Strength Anti-fungal Formula

NDC Package 80569-101-15 Crystal Flush Maximum Strength Anti-fungal Formula

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
80569-101-15
Package Description:
15 mL in 1 BOTTLE
Product Code:
80569-101
Proprietary Name:
Crystal Flush Maximum Strength Anti-fungal Formula
Usage Information:
Clean or wash the affected area and dry throughly. Apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by doctor. For athletes foot, pay special attention to space between toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails. Supervise children in the use of this product.
11-Digit NDC Billing Format:
80569010115
NDC to RxNorm Crosswalk:
  • RxCUI: 313423 - tolnaftate 1 % Topical Solution
  • RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution
    • Labeler Name:
    Triple Point Group, Llc
    Sample Package:
    No
    Start Marketing Date:
    04-07-2021
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 80569-101-15?

    The NDC Packaged Code 80569-101-15 is assigned to a package of 15 ml in 1 bottle of Crystal Flush Maximum Strength Anti-fungal Formula, labeled by Triple Point Group, Llc. The product's dosage form is and is administered via form.

    Is NDC 80569-101 included in the NDC Directory?

    No, Crystal Flush Maximum Strength Anti-fungal Formula with product code 80569-101 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Triple Point Group, Llc on April 07, 2021 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 80569-101-15?

    The 11-digit format is 80569010115. 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
    5-3-280569-101-155-4-280569-0101-15