NDC 75902-6001 Dio Enamel Coating Pen Pro Tooth
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75902 - Dio Corporation
- 75902-6001 - Dio Enamel Coating Pen Pro Tooth
Product Packages
NDC Code 75902-6001-1
Package Description: 5 g in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 75902-6001?
What are the uses for Dio Enamel Coating Pen Pro Tooth?
Which are Dio Enamel Coating Pen Pro Tooth UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Dio Enamel Coating Pen Pro Tooth 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:
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
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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".