NDC 73557-135 Csi Cooling 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:
73557-135
Proprietary Name:
Csi Cooling Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shanghai Chuangshi Industry Group Co., Ltd
Labeler Code:
73557
Start Marketing Date: [9]
01-28-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 73557-135-05

Package Description: 5 PACKAGE in 1 BOX / 1 g in 1 PACKAGE (73557-135-01)

Product Details

What is NDC 73557-135?

The NDC code 73557-135 is assigned by the FDA to the product Csi Cooling Patch which is product labeled by Shanghai Chuangshi Industry Group Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73557-135-05 5 package in 1 box / 1 g in 1 package (73557-135-01). 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 Csi Cooling Patch?

* Adult and Children 12 year of age and older: Clean and dry affected area, partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. * Children under 12 years of age: Consult physician.

Which are Csi Cooling Patch UNII Codes?

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

Which are Csi Cooling 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".