NDC 24653-816 Face Guard 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 24653-816?
What are the uses for Face Guard 15?
Which are Face Guard 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Face Guard 15 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BISOCTRIZOLE (UNII: 8NT850T0YS)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- STEARETH-21 (UNII: 53J3F32P58)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ECTOINE (UNII: 7GXZ3858RY)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- GLYCERETH-17 STEARATE (UNII: 02R46S8KUH)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- EDETIC ACID (UNII: 9G34HU7RV0)
- PROPYLENE (UNII: AUG1H506LY)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
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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".