NDC 81048-008 Chewpaste With Fluoride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81048 - 2557807 Ontario Inc
- 81048-008 - Chewpaste With Fluoride
Product Characteristics
Product Packages
NDC Code 81048-008-64
Package Description: 64 TABLET, CHEWABLE in 1 JAR
NDC Code 81048-008-92
Package Description: 192 TABLET, CHEWABLE in 1 JAR
Product Details
What is NDC 81048-008?
What are the uses for Chewpaste With Fluoride?
Which are Chewpaste With Fluoride 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 Chewpaste With Fluoride 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- KAOLIN (UNII: 24H4NWX5CO)
- XYLITOL (UNII: VCQ006KQ1E)
- ERYTHRITOL (UNII: RA96B954X6)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- MINT (UNII: FV98Z8GITP)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- BENTONITE (UNII: A3N5ZCN45C)
- VANILLA BEAN (UNII: Q74T35078H)
- EUCALYPTOL (UNII: RV6J6604TK)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
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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".