NDC 54162-250 Tera-gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Llc
- 54162-250 - Tera-gel
Product Packages
NDC Code 54162-250-04
Package Description: 114 mL in 1 BOTTLE, PLASTIC
NDC Code 54162-250-80
Package Description: 237 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54162-250?
What are the uses for Tera-gel?
Which are Tera-gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are Tera-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:
- WATER (UNII: 059QF0KO0R)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Tera-gel?
- RxCUI: 284305 - Tera Gel 0.5 % Medicated Shampoo
- RxCUI: 284305 - coal tar 5 MG/ML Medicated Shampoo [Tera Gel]
- RxCUI: 284305 - Tera Gel 5 MG/ML Medicated Shampoo
- RxCUI: 309381 - coal tar 0.5 % Medicated Shampoo
- RxCUI: 309381 - coal tar 5 MG/ML Medicated Shampoo
* 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".