NDC 54162-550 Men-phor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Llc
- 54162-550 - Men-phor
Product Packages
NDC Code 54162-550-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 54162-550-07
Package Description: 222 mL in 1 BOTTLE, PUMP
NDC Code 54162-550-09
Package Description: 222 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 54162-550?
What are the uses for Men-phor?
Which are Men-phor UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Men-phor 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)
- ALCOHOL (UNII: 3K9958V90M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PEG-200 DILAURATE (UNII: TWV5J70L88)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- PETROLATUM (UNII: 4T6H12BN9U)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Men-phor?
- RxCUI: 200176 - camphor 0.5 % / menthol 0.5 % Topical Lotion
- RxCUI: 200176 - camphor 5 MG/ML / menthol 5 MG/ML Topical Lotion
- RxCUI: 605666 - Men-phor 0.5 % / 0.5 % Topical Lotion
- RxCUI: 605666 - camphor 5 MG/ML / menthol 5 MG/ML Topical Lotion [Men-phor]
- RxCUI: 605666 - Men-phor (camphor 0.5 % / menthol 0.5 % ) Topical Lotion
* 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".