NDC 53462-561 Suction Toothbrush With Corinz Oral Rinse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53462 - Sage Products, Llc
- 53462-561 - Suction Toothbrush With Corinz Oral Rinse
Product Packages
NDC Code 53462-561-60
Package Description: 1 KIT in 1 KIT * 1 PACKET in 1 KIT / 7 mL in 1 PACKET (53462-375-60)
Product Details
What is NDC 53462-561?
What are the uses for Suction Toothbrush With Corinz Oral Rinse?
Which are Suction Toothbrush With Corinz Oral Rinse UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CETYLPYRIDINIUM (UNII: CUB7JI0JV3) (Active Moiety)
Which are Suction Toothbrush With Corinz Oral Rinse 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- XYLITOL (UNII: VCQ006KQ1E)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
What is the NDC to RxNorm Crosswalk for Suction Toothbrush With Corinz Oral Rinse?
- RxCUI: 1251617 - cetylpyridinium chloride 0.05 % Mouthwash
- RxCUI: 1251617 - cetylpyridinium chloride 0.5 MG/ML Mouthwash
- RxCUI: 1251788 - cetylpyridinium chloride 0.05 % Mucous Membrane Topical Solution
- RxCUI: 1251788 - cetylpyridinium chloride 0.5 MG/ML Mucous Membrane Topical Solution
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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".