NDC 73573-005 Reddyport Antiplaque Solution
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73573 - Smd Manufacturing
- 73573-005 - Reddyport Antiplaque Solution
Product Packages
NDC Code 73573-005-15
Package Description: 14.8 mL in 1 CUP
Product Details
What is NDC 73573-005?
What are the uses for Reddyport Antiplaque Solution?
Which are Reddyport Antiplaque Solution UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CETYLPYRIDINIUM (UNII: CUB7JI0JV3) (Active Moiety)
Which are Reddyport Antiplaque Solution 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:
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
- SPEARMINT (UNII: J7I2T6IV1N)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL SOLUTION 70% (UNII: 8KW3E207O2)
What is the NDC to RxNorm Crosswalk for Reddyport Antiplaque Solution?
- RxCUI: 1251617 - cetylpyridinium chloride 0.05 % Mouthwash
- RxCUI: 1251617 - cetylpyridinium chloride 0.5 MG/ML Mouthwash
- RxCUI: 358975 - hydrogen peroxide 1.5 % Mouthwash
- RxCUI: 358975 - hydrogen peroxide 15 MG/ML Mouthwash
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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".