NDC 71275-001 Burst Wonderfully Whitening Anti Cavity
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71275 - Burst.usa.inc
- 71275-001 - Burst
Product Characteristics
Product Packages
NDC Code 71275-001-47
Package Description: 133 g in 1 TUBE
Product Details
What is NDC 71275-001?
What are the uses for Burst Wonderfully Whitening Anti Cavity?
Which are Burst Wonderfully Whitening Anti Cavity 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 Burst Wonderfully Whitening Anti Cavity 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TRICLOSAN (UNII: 4NM5039Y5X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Burst Wonderfully Whitening Anti Cavity?
- 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
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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".