NDC 0041-1421 Oral-b Anticavity
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0041 - Oral-b Laboratories
- 0041-1421 - Oral-b
Product Characteristics
Product Packages
NDC Code 0041-1421-16
Package Description: 500 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 0041-1421?
What are the uses for Oral-b Anticavity?
Which are Oral-b Anticavity UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Oral-b Anticavity?
- RxCUI: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
- RxCUI: 240698 - sodium fluoride 0.5 MG/ML Mouthwash
- RxCUI: 831841 - Oral-B Anticavity 0.05 % Oral Rinse
- RxCUI: 831841 - sodium fluoride 0.5 MG/ML Mouthwash [Oral B Anti-Cavity]
- RxCUI: 831841 - Oral B Anti-Cavity 0.05 % Mouthwash
* 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".