NDC 75140-002 Kaydia Patch

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:
75140-002
Proprietary Name:
Kaydia Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Strong Current Enterprises Limited
Labeler Code:
75140
Start Marketing Date: [9]
05-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75140-002-01

Package Description: 166 g in 1 BOX

Product Details

What is NDC 75140-002?

The NDC code 75140-002 is assigned by the FDA to the product Kaydia Patch which is product labeled by Strong Current Enterprises Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75140-002-01 166 g in 1 box . 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 Kaydia Patch?

1.Remove backing film 2.Apply patch on dry and clean skin 3.Remove and discard patch after 8-10 hours

Which are Kaydia Patch UNII Codes?

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

Which are Kaydia Patch 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:

* Please review the disclaimer below.

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".