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  4. NDC Product Code: 76772-022 Luxury

NDC 76772-022 Luxury

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76772-022?
  4. Luxury Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76772-022
Proprietary Name:
Luxury
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi
Labeler Code:
76772
Product Label ID:
61ded99e-970e-4c61-8b61-1cac61e309da
Start Marketing Date: [9]
03-10-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 76772-022?

The NDC code 76772-022 is assigned by the FDA to the product Luxury which is product labeled by Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76772-022-57 57 g in 1 canister . 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 Luxury?

Shake can well and spray a thin layer over affected area twice daily (morning and night)wash affected area and dry thoroughlyhold can 4-6 inches away from affected areasupervise children in the use of this productfor athlete's foot, pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyuse daily for 4 weeks; if condition persists longer, ask a doctorif condition persists longer, consult a doctorthis product is not effective on the scalp or nailsin case of  clogging , clean nozzle with a pin

Which are Luxury UNII Codes?

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

Which are Luxury 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".