NDC 72914-0002 Relief And Cooling
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 72914-0002?
What are the uses for Relief And Cooling?
Which are Relief And Cooling UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Relief And Cooling 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:
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- 2-(2-(2-(2-PHENOXYETHOXY)ETHOXY)ETHOXY)ETHANOL (UNII: Y050HYR4XA)
- WATER (UNII: 059QF0KO0R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- EDETIC ACID (UNII: 9G34HU7RV0)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
What is the NDC to RxNorm Crosswalk for Relief And Cooling?
- RxCUI: 1655936 - menthol 3.7 % Topical Cream
- RxCUI: 1655936 - menthol 37 MG/ML Topical Cream
* 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".