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  5. NDC Package Code: 80569-184-15 Crystal Flush Maximum Strength Anti-fungal Formula

NDC Package 80569-184-15 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:
80569-184-15
Package Description:
15 mL in 1 BOTTLE
Product Code:
80569-184
Proprietary Name:
Crystal Flush Maximum Strength Anti-fungal Formula
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:
80569018415
NDC to RxNorm Crosswalk:
Labeler Name:
Triple Point Group, Llc
Sample Package:
No
FDA Application Number:
part333C
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
09-17-2020
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 80569-184-15?

The NDC Packaged Code 80569-184-15 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 80569-184 included in the NDC Directory?

No, Crystal Flush Maximum Strength Anti-fungal Formula with product code 80569-184 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 September 17, 2020 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 80569-184-15?

The 11-digit format is 80569018415. 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
5-3-280569-184-155-4-280569-0184-15