NDC 68828-117 Skin Defense Concealer Broad Spectrum Spf 15 Jafra Cosmetics
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What is NDC 68828-117?
What are the uses for Skin Defense Concealer Broad Spectrum Spf 15 Jafra Cosmetics?
Which are Skin Defense Concealer Broad Spectrum Spf 15 Jafra Cosmetics UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Skin Defense Concealer Broad Spectrum Spf 15 Jafra Cosmetics 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- DI-PPG-3 MYRISTYL ETHER ADIPATE (UNII: T32481VTXW)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- TROLAMINE (UNII: 9O3K93S3TK)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALFALFA (UNII: DJO934BRBD)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SWEET POTATO (UNII: M9WGG9Z9GK)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".