NDC 74438-010 Tlcuo Pure

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:
74438-010
Proprietary Name:
Tlcuo Pure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ktl Ltd
Labeler Code:
74438
Start Marketing Date: [9]
03-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74438-010-01

Package Description: 60 mL in 1 BOTTLE, SPRAY

NDC Code 74438-010-02

Package Description: 500 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 74438-010?

The NDC code 74438-010 is assigned by the FDA to the product Tlcuo Pure which is product labeled by Ktl Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74438-010-01 60 ml in 1 bottle, spray , 74438-010-02 500 ml in 1 bottle, spray . 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 Tlcuo Pure?

Directions:Take an appropriate amount on your hands and rub thoroughly to dry.Rub evenly over areas of your hands or feet to dry naturally. For infants, the skin is weak and sensitive, preferably not to be used.

Which are Tlcuo Pure UNII Codes?

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

Which are Tlcuo Pure 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".