NDC 68927-3492 Fungazoil Advanced

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:
68927-3492
Proprietary Name:
Fungazoil Advanced
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pedifix
Labeler Code:
68927
Start Marketing Date: [9]
06-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68927-3492-1

Package Description: 15 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 68927-3492?

The NDC code 68927-3492 is assigned by the FDA to the product Fungazoil Advanced which is product labeled by Pedifix. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68927-3492-1 15 ml in 1 bottle, with applicator . 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 Fungazoil Advanced?

Read all package directions and warnings before using.• Use only as directed.• Clean the affected area with soap and warm water and dry thoroughly.• Apply a thin layer over the affected area twice daily (morning and night) or as directed by a doctor.• This product is not effective on the scalp or nails.• Avoid applying to severely cracked or irritated areas.• For athlete’s foot: pay special attention to spaces 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.• Super vise children in the use of this product.• Intended for use by normally healthy adults only.• Persons under 18 years of age or those with sensitive or allergic skin should use only as directed by a doctor.Other InformationApply to skin around affected areas. While not all finger and toe fungal infections are curable with OTC topical medications, if you see improvement within 4 weeks of use, you may continue to use until satisfactory results are obtained.

Which are Fungazoil Advanced UNII Codes?

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

Which are Fungazoil Advanced 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 Fungazoil Advanced?

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".