NDC 54162-540 Keratek
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Corp
- 54162-540 - Keratek
Product Packages
NDC Code 54162-540-04
Package Description: 113 g in 1 BOTTLE
Product Details
What is NDC 54162-540?
What are the uses for Keratek?
Which are Keratek UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Keratek 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:
- ARNICA MONTANA (UNII: O80TY208ZW)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LANOLIN (UNII: 7EV65EAW6H)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Keratek?
- RxCUI: 1441111 - menthol 16 % / methyl salicylate 28 % Topical Gel
- RxCUI: 1441111 - menthol 0.16 MG/MG / methyl salicylate 0.28 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".