NDC 80569-184 Crystal Flush Maximum Strength Anti-fungal Formula

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80569-184
Proprietary Name:
Crystal Flush Maximum Strength Anti-fungal Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Triple Point Group, Llc
Labeler Code:
80569
Start Marketing Date: [9]
09-17-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80569-184-15

Package Description: 15 mL in 1 BOTTLE

Product Details

What is NDC 80569-184?

The NDC code 80569-184 is assigned by the FDA to the product Crystal Flush Maximum Strength Anti-fungal Formula which is product labeled by Triple Point Group, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80569-184-15 15 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Crystal Flush Maximum Strength Anti-fungal Formula?

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.

Which are Crystal Flush Maximum Strength Anti-fungal Formula UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Crystal Flush Maximum Strength Anti-fungal Formula Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Crystal Flush Maximum Strength Anti-fungal Formula?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".