NDC 51815-214 Right Guard Total Defense 5 Arctic Refresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51815 - Vvf Illinois Services Llc
- 51815-214 - Right Guard Total Defense 5
Product Packages
NDC Code 51815-214-00
Package Description: 113 g in 1 APPLICATOR
NDC Code 51815-214-01
Package Description: 85 g in 1 APPLICATOR
Product Details
What is NDC 51815-214?
What are the uses for Right Guard Total Defense 5 Arctic Refresh?
Which are Right Guard Total Defense 5 Arctic Refresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY)
- ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (Active Moiety)
Which are Right Guard Total Defense 5 Arctic Refresh 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)
- ALCOHOL (UNII: 3K9958V90M)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- 2-BENZYLHEPTANOL (UNII: 344745V05R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".