NDC 69851-101 Therapeutic Icy Cold Cooling Pain Relief Roll-on
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69851 - Apex-carex Heathcare Products
- 69851-101 - Therapeutic Icy Cold
Product Packages
NDC Code 69851-101-13
Package Description: 88.8 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 69851-101?
What are the uses for Therapeutic Icy Cold Cooling Pain Relief Roll-on?
Which are Therapeutic Icy Cold Cooling Pain Relief Roll-on 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 Roll-on 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 Roll-on?
- RxCUI: 1486765 - menthol 3.9 % Topical Gel
- RxCUI: 1486765 - menthol 0.039 MG/MG Topical Gel
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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".