NDC 52301-365 Kool Comfort
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52301 - Dee Cee Laboratories, Inc.
- 52301-365 - Kool Comfort
Product Packages
NDC Code 52301-365-08
Package Description: 226.79 g in 1 JAR
NDC Code 52301-365-16
Package Description: 453.59 g in 1 JAR
NDC Code 52301-365-32
Package Description: 907.2 g in 1 JAR
NDC Code 52301-365-78
Package Description: 2211.22 g in 1 JAR
Product Details
What is NDC 52301-365?
What are the uses for Kool Comfort?
Which are Kool Comfort UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Kool Comfort 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:
- CARBOMER 934 (UNII: Z135WT9208)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- EDETOL (UNII: Q4R969U9FR)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
What is the NDC to RxNorm Crosswalk for Kool Comfort?
- RxCUI: 1356543 - Kool Comfort 2.5 % Topical Gel
- RxCUI: 1356543 - menthol 0.025 MG/MG Topical Gel [Kool Comfort]
- RxCUI: 1356543 - Kool Comfort 0.025 MG/MG Topical Gel
- RxCUI: 282805 - menthol 2.5 % Topical Gel
- RxCUI: 282805 - menthol 0.025 MG/MG Topical Gel
* Please review the disclaimer below.
[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".