NDC 67225-0010 2080 Dentistry Night Repair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67225 - Aekyung Industrial Co., Ltd.
- 67225-0010 - 2080 Dentistry Night Repair
Product Packages
NDC Code 67225-0010-1
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Details
What is NDC 67225-0010?
What are the uses for 2080 Dentistry Night Repair?
Which are 2080 Dentistry Night Repair UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are 2080 Dentistry Night Repair 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:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CALCIUM GLYCEROPHOSPHATE (UNII: XWV9Z12C1C)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- SORBITOL (UNII: 506T60A25R)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- WATER (UNII: 059QF0KO0R)
* 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".