NDC 54157-108 Upc 801803 00203 Megafresh Fluoride Tooth
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54157 - American Amenities, Inc.
- 54157-108 - Upc 801803 00203 Megafresh Fluoride Tooth
Product Packages
NDC Code 54157-108-01
Package Description: 17 g in 1 TUBE
NDC Code 54157-108-02
Package Description: 24 g in 1 TUBE
NDC Code 54157-108-03
Package Description: 43 g in 1 TUBE
NDC Code 54157-108-04
Package Description: 78 g in 1 TUBE
NDC Code 54157-108-05
Package Description: 85 g in 1 TUBE
NDC Code 54157-108-06
Package Description: 130 g in 1 TUBE
NDC Code 54157-108-07
Package Description: 181 g in 1 TUBE
NDC Code 54157-108-08
Package Description: 200 g in 1 TUBE
NDC Code 54157-108-09
Package Description: 4.25 g in 1 POUCH
Product Details
What is NDC 54157-108?
What are the uses for Upc 801803 00203 Megafresh Fluoride Tooth?
Which are Upc 801803 00203 Megafresh Fluoride Tooth UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Upc 801803 00203 Megafresh Fluoride Tooth 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)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- GUAR GUM (UNII: E89I1637KE)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Upc 801803 00203 Megafresh Fluoride Tooth?
- RxCUI: 1091932 - sodium monofluorophosphate 0.1 % Toothpaste
- RxCUI: 1091932 - sodium monofluorophosphate 0.001 MG/MG Toothpaste
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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".