NDC 68828-147 Skin Defense Makeup Spf-15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68828-147?
What are the uses for Skin Defense Makeup Spf-15?
Which are Skin Defense Makeup Spf-15 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 Makeup Spf-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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- DI-PPG-3 MYRISTYL ETHER ADIPATE (UNII: T32481VTXW)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- METHYL METHACRYLATE (UNII: 196OC77688)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TREHALOSE (UNII: B8WCK70T7I)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- POLIDRONIUM CHLORIDE (UNII: 6716Z5YR3G)
- UREA (UNII: 8W8T17847W)
- GLYCERIN (UNII: PDC6A3C0OX)
- OAT (UNII: Z6J799EAJK)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TROLAMINE (UNII: 9O3K93S3TK)
- TAGETES ERECTA FLOWER (UNII: UH5X33P33E)
- IPOMOEA MAURITIANA TUBER (UNII: K67Y2SGX79)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- POVIDONE K30 (UNII: U725QWY32X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 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".