NDC 24653-830 Face Guard 30 Spf
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What is NDC 24653-830?
What are the uses for Face Guard 30 Spf?
Which are Face Guard 30 Spf UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Face Guard 30 Spf 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- DI-C12-15 ALKYL FUMARATE (UNII: A1CB3Z898P)
- GLUCAMETACIN (UNII: N1EXE5EHAN)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- STEARETH-21 (UNII: 53J3F32P58)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BISOCTRIZOLE (UNII: 8NT850T0YS)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- ECTOINE (UNII: 7GXZ3858RY)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
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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".