NDC 11822-4217 Rite Aid Cool Therapy Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-4217 - Rite Aid Cool Therapy Gel
Product Packages
NDC Code 11822-4217-1
Package Description: 88.72 mL in 1 BOTTLE
Product Details
What is NDC 11822-4217?
What are the uses for Rite Aid Cool Therapy Gel?
Which are Rite Aid Cool Therapy Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Rite Aid Cool Therapy Gel 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Rite Aid Cool Therapy Gel?
- RxCUI: 415974 - menthol 4 % Topical Gel
- RxCUI: 415974 - menthol 0.04 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".