NDC 73076-114 Lmnoop Athletes Foot Cream

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:
73076-114
Proprietary Name:
Lmnoop Athletes Foot Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Ishan Technology Co., Ltd
Labeler Code:
73076
Start Marketing Date: [9]
12-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73076-114-01

Package Description: 50 g in 1 TUBE

Product Details

What is NDC 73076-114?

The NDC code 73076-114 is assigned by the FDA to the product Lmnoop Athletes Foot Cream which is product labeled by Shenzhen Ishan Technology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73076-114-01 50 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 Lmnoop Athletes Foot Cream?

* Clean the affected area and dry thoroughly * Apply a thin layer of LMNOOP over affected area twice daily (morning and night) or as directed by a doctor. * Use daily for 4 weeks, pay special attention to the spaces between the toes; wear well-fitting ventilated shoes, and change shoes and socks at least once daily. * Supervise children in the use of this product. * Wash hands after each use.

Which are Lmnoop Athletes Foot Cream UNII Codes?

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

Which are Lmnoop Athletes Foot Cream 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".