NDC 69851-102 Therapeutic Icy Cold Cooling Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69851 - Apex-carex Heathcare Products
- 69851-102 - Therapeutic Icy Cold
Product Packages
NDC Code 69851-102-24
Package Description: 118 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 69851-102?
What are the uses for Therapeutic Icy Cold Cooling Pain Relief?
Which are Therapeutic Icy Cold Cooling Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Therapeutic Icy Cold Cooling Pain Relief 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- UNCARIA TOMENTOSA LEAF (UNII: 487U8M3D2P)
- BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
What is the NDC to RxNorm Crosswalk for Therapeutic Icy Cold Cooling Pain Relief?
- RxCUI: 259550 - menthol 6 % Topical Spray
- RxCUI: 259550 - menthol 60 MG/ML Topical Spray
* 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".