NDC 69638-066 Scotts Select Apf Foam Fluoride

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:
69638-066
Proprietary Name:
Scotts Select Apf Foam Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Scott's Dental Supply Llc
Labeler Code:
69638
Start Marketing Date: [9]
04-22-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
STRAWBERRY (C73417)

Product Packages

NDC Code 69638-066-44

Package Description: 130 mL in 1 BOTTLE

Product Details

What is NDC 69638-066?

The NDC code 69638-066 is assigned by the FDA to the product Scotts Select Apf Foam Fluoride which is product labeled by Scott's Dental Supply Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69638-066-44 130 ml in 1 bottle . 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 Scotts Select Apf Foam Fluoride?

Remove cap from can. Prior to each use, shake can thoroughly for at least 15 seconds.To dispense, invert the can completely upside down. Slowly depress nozzle to dispense foam into a fluoride tray (foam will expand slightly higher than fluoride tray).Air dry teeth thoroughly and insert tray(s) into patient's mouth. Instruct patient to bite down and leave the tray in contact with the teeth between 1 - 4 minutes.Use a saliva ejector during treatment to minimize ingestion of product.Remove tray(s) and have patient expectorate.Instruct patient not to eat, drink or rinse for 30 minutes after treatment.

Which are Scotts Select Apf Foam Fluoride UNII Codes?

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

Which are Scotts Select Apf Foam Fluoride 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 Scotts Select Apf Foam Fluoride?

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:

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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".