NDC 73557-135 Csi Cooling Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73557 - Shanghai Chuangshi Industry Group Co., Ltd
- 73557-135 - Csi Cooling Patch
Product Characteristics
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?
What are the uses for Csi Cooling Patch?
Which are Csi Cooling Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
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:
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONE K30 (UNII: U725QWY32X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- KAOLIN (UNII: 24H4NWX5CO)
- TARTARIC ACID (UNII: W4888I119H)
- WATER (UNII: 059QF0KO0R)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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[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".