NDC 51460-1112 Amerfresh

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51460-1112
Proprietary Name:
Amerfresh
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amercare Products, Inc.
Labeler Code:
51460
Start Marketing Date: [9]
11-14-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404)

Product Packages

NDC Code 51460-1112-0

Package Description: 142 g in 1 TUBE

NDC Code 51460-1112-1

Package Description: 85 g in 1 TUBE

NDC Code 51460-1112-2

Package Description: 7.1 g in 1 PACKET

NDC Code 51460-1112-3

Package Description: 1 TUBE in 1 BOX / 85 g in 1 TUBE

NDC Code 51460-1112-4

Package Description: 17 g in 1 TUBE

NDC Code 51460-1112-5

Package Description: 24 g in 1 TUBE

NDC Code 51460-1112-6

Package Description: 43 g in 1 TUBE

NDC Code 51460-1112-7

Package Description: 1 TUBE in 1 BOX / 43 g in 1 TUBE

NDC Code 51460-1112-8

Package Description: 130 g in 1 TUBE

NDC Code 51460-1112-9

Package Description: 181 g in 1 TUBE

Product Details

What is NDC 51460-1112?

The NDC code 51460-1112 is assigned by the FDA to the product Amerfresh which is product labeled by Amercare Products, Inc.. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 51460-1112-0 142 g in 1 tube , 51460-1112-1 85 g in 1 tube , 51460-1112-2 7.1 g in 1 packet , 51460-1112-3 1 tube in 1 box / 85 g in 1 tube, 51460-1112-4 17 g in 1 tube , 51460-1112-5 24 g in 1 tube , 51460-1112-6 43 g in 1 tube , 51460-1112-7 1 tube in 1 box / 43 g in 1 tube, 51460-1112-8 130 g in 1 tube , 51460-1112-9 181 g in 1 tube . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Amerfresh?

Do not swallowsupervise children as necessary until capable of using without supervisionInstruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing).Adults and children 6 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or a doctor.Children under 6 years of age: Do not use unless directed by a doctor or dentist

Which are Amerfresh UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Amerfresh 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:

What is the NDC to RxNorm Crosswalk for Amerfresh?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste

* Please review the disclaimer below.

Product Footnotes

[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".