NDC 64778-1375 Denti-care Topical Fluoride Foam Grape
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64778 - Ar Medicom Inc
- 64778-1375 - Denti-care
Product Characteristics
Product Packages
NDC Code 64778-1375-1
Package Description: 125 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 64778-1375?
Which are Denti-care Topical Fluoride Foam Grape UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
What is the NDC to RxNorm Crosswalk for Denti-care Topical Fluoride Foam Grape?
- RxCUI: 1090053 - sodium fluoride 1.76 % / hydrofluoric acid 1.04 % Oral Foam
- RxCUI: 1090053 - hydrofluoric acid 10.4 MG/ML / sodium fluoride 17.6 MG/ML Oral Foam
- RxCUI: 1090053 - hydrofluoric acid 1.04 % / sodium fluoride 1.76 % (fluoride ion 1.23 % ) Oral Foam
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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".