NDC 54157-104 Megafresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 54157-104-01
Package Description: 17 g in 1 TUBE
NDC Code 54157-104-02
Package Description: 24 g in 1 TUBE
NDC Code 54157-104-03
Package Description: 35 g in 1 TUBE
NDC Code 54157-104-04
Package Description: 43 g in 1 TUBE
NDC Code 54157-104-05
Package Description: 50 g in 1 TUBE
NDC Code 54157-104-06
Package Description: 70 g in 1 TUBE
NDC Code 54157-104-07
Package Description: 78 g in 1 TUBE
NDC Code 54157-104-08
Package Description: 90 g in 1 TUBE
NDC Code 54157-104-09
Package Description: 100 g in 1 TUBE
NDC Code 54157-104-10
Package Description: 120 g in 1 TUBE
NDC Code 54157-104-11
Package Description: 130 g in 1 TUBE
NDC Code 54157-104-12
Package Description: 150 g in 1 TUBE
NDC Code 54157-104-13
Package Description: 181 g in 1 TUBE
NDC Code 54157-104-14
Package Description: 200 g in 1 TUBE
NDC Code 54157-104-15
Package Description: 4.25 g in 1 POUCH
NDC Code 54157-104-16
Package Description: 3 g in 1 POUCH
NDC Code 54157-104-17
Package Description: 5 g in 1 POUCH
NDC Code 54157-104-18
Package Description: 10 g in 1 POUCH
NDC Code 54157-104-19
Package Description: 71 g in 1 TUBE
NDC Code 54157-104-20
Package Description: 85 g in 1 TUBE
Product Details
What is NDC 54157-104?
What are the uses for Megafresh?
Which are Megafresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Megafresh 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)
- SORBITOL (UNII: 506T60A25R)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Megafresh?
- RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
- RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste
* 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".