NDC 69729-064 Lakesia

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:
69729-064
Proprietary Name:
Lakesia
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Opmx Llc
Labeler Code:
69729
Start Marketing Date: [9]
07-02-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69729-064-20

Package Description: 1 TUBE in 1 BOX / 20 g in 1 TUBE

Product Details

What is NDC 69729-064?

The NDC code 69729-064 is assigned by the FDA to the product Lakesia which is product labeled by Opmx Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69729-064-20 1 tube in 1 box / 20 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 Lakesia?

Wash affected area and dry thoroughlyapply a thin layer cover affected area twice daily (morning and night) or as directed by a doctorsupervise 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 a dayfor athlete's foot and ringworm use daily for 4 weeks, for jock itch use daily for 2 weeks if conditions persist longer, ask a doctorthis product is not effective on the scalp or nails

Which are Lakesia UNII Codes?

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

Which are Lakesia 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".