NDC 51460-5010 Amerfresh Clear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51460 - Amercare Products Inc
- 51460-5010 - Amerfresh Clear
Product Characteristics
Product Packages
NDC Code 51460-5010-1
Package Description: 85 g in 1 TUBE
NDC Code 51460-5010-2
Package Description: 42 g in 1 TUBE
NDC Code 51460-5010-3
Package Description: 24 g in 1 TUBE
NDC Code 51460-5010-4
Package Description: 17 g in 1 TUBE
NDC Code 51460-5010-5
Package Description: 181 g in 1 TUBE
Product Details
What is NDC 51460-5010?
What are the uses for Amerfresh Clear?
Which are Amerfresh Clear 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 Amerfresh Clear 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:
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
What is the NDC to RxNorm Crosswalk for Amerfresh Clear?
- RxCUI: 245598 - sodium fluoride 0.22 % Toothpaste
- RxCUI: 245598 - sodium fluoride 0.0022 MG/MG Toothpaste
- RxCUI: 245598 - sodium fluoride 0.22 % (fluoride 0.1 % ) 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".