NDC 24653-283 Face Guard Advanced
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24653 - Janssen Cosmetics Gmbh
- 24653-283 - Face Guard Advanced
Product Packages
NDC Code 24653-283-02
Package Description: 1 BOTTLE, PUMP in 1 BOX / 30 mL in 1 BOTTLE, PUMP (24653-283-01)
Product Details
What is NDC 24653-283?
What are the uses for Face Guard Advanced?
Which are Face Guard Advanced UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Face Guard Advanced 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- GLYCERIN (UNII: PDC6A3C0OX)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BISOCTRIZOLE (UNII: 8NT850T0YS)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- STEARETH-21 (UNII: 53J3F32P58)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- THERMUS THERMOPHILUS (UNII: 415H64SACF)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- ECTOINE (UNII: 7GXZ3858RY)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLENE GLYCOL MONOLAURATE (UNII: 2Z947R568V)
* 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".