NDC 0273-7004 Perfect Choice
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What is NDC 0273-7004?
What are the uses for Perfect Choice?
Which are Perfect Choice 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 Perfect Choice?
- RxCUI: 1297381 - hydrofluoric acid 1 % / phosphoric acid 1.12 % / sodium fluoride 1.8 % Oral Gel
- RxCUI: 1297381 - hydrofluoric acid 0.01 MG/MG / phosphoric acid 0.0112 MG/MG / sodium fluoride 0.018 MG/MG Oral Gel
- RxCUI: 1297387 - perfectchoice One Minute 1.23 % Oral Gel
- RxCUI: 1297387 - hydrofluoric acid 0.01 MG/MG / phosphoric acid 0.0112 MG/MG / sodium fluoride 0.018 MG/MG Oral Gel [Perfect Choice One Minute]
- RxCUI: 1297387 - Perfect Choice One Minute (hydrofluoric acid 1 % / phosphoric acid 1.12 % / sodium fluoride 1.8 % ) Oral Gel
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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".