NDC 55316-829 Healthy Accents Antifungal

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:
55316-829
Proprietary Name:
Healthy Accents Antifungal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dza Brands Llc
Labeler Code:
55316
Start Marketing Date: [9]
07-26-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55316-829-28

Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE

Product Details

What is NDC 55316-829?

The NDC code 55316-829 is assigned by the FDA to the product Healthy Accents Antifungal which is product labeled by Dza Brands Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55316-829-28 1 tube in 1 carton / 28 g in 1 tube. 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 Healthy Accents Antifungal?

Directionswash affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night)supervise children in the use of this productfor athlete's foot: pay special attention to spaces between the toes, wear well-fitting, ventilated shoes and chagne shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeksif condtion persists longer, ask a doctorthis product is not effectiveo n the scalp or nails

Which are Healthy Accents Antifungal UNII Codes?

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

Which are Healthy Accents Antifungal 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:

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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".