NDC 24765-100 Dental Clear Natural
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24765 - Pharmacal-international. Co., Ltd.
- 24765-100 - Dental Clear Natural
Product Packages
NDC Code 24765-100-01
Package Description: 260 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 24765-100?
What are the uses for Dental Clear Natural?
Which are Dental Clear Natural UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Dental Clear Natural 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)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- GLYCERIN (UNII: PDC6A3C0OX)
- ACETIC ACID (UNII: Q40Q9N063P)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- CAMELLIA SINENSIS ROOT (UNII: 8H54O0V2K3)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- XYLITOL (UNII: VCQ006KQ1E)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)
- MALIC ACID (UNII: 817L1N4CKP)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
What is the NDC to RxNorm Crosswalk for Dental Clear Natural?
- RxCUI: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
- RxCUI: 240698 - sodium fluoride 0.5 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".