NDC 69491-831 Crest
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69491 - Buzz Export Services Pty., Ltd.
- 69491-831 - Crest
Product Packages
NDC Code 69491-831-01
Package Description: 1 TUBE in 1 CARTON / 24 g in 1 TUBE
Product Details
What is NDC 69491-831?
What are the uses for Crest?
Which are Crest 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 Crest 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)
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM LAURETH-2 PHOSPHATE (UNII: 1IO8CC3XDG)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- POLYETHYLENE OXIDE 900000 (UNII: 16P9295IIL)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Crest?
- RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
- RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste
* Please review the disclaimer below.
Patient Education
Fluoride
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* 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".