NDC 20890-0020 Lander Polar Ice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20890 - Abaco Partners Llc Dba Surefil
- 20890-0020 - Lander
Product Characteristics
Product Packages
NDC Code 20890-0020-1
Package Description: 226 g in 1 CONTAINER
Product Details
What is NDC 20890-0020?
What are the uses for Lander Polar Ice?
Which are Lander Polar Ice UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Lander Polar Ice 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Lander Polar Ice?
- RxCUI: 311502 - menthol 2 % Topical Gel
- RxCUI: 311502 - menthol 0.02 MG/MG Topical Gel
- RxCUI: 311502 - menthol 2 % topical stick
* 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".