NDC 52099-8000 Freezin Cold Toast
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52099 - Q.a. Laboratories
- 52099-8000 - Freezin Cold Toast
Product Packages
NDC Code 52099-8000-1
Package Description: 141 g in 1 TUBE
Product Details
What is NDC 52099-8000?
What are the uses for Freezin Cold Toast?
Which are Freezin Cold Toast UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Freezin Cold Toast 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TRIDECETH-10 (UNII: G624N6MSBA)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- ROSEMARY (UNII: IJ67X351P9)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Freezin Cold Toast?
- RxCUI: 1300276 - menthol 11 % / methyl salicylate 31 % Topical Cream
- RxCUI: 1300276 - menthol 110 MG/ML / methyl salicylate 310 MG/ML Topical Cream
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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".