NDC 76351-100 Tinted Moisturizer Spf-15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76351 - Femme Couture International, Inc
- 76351-100 - Tinted Moisturizer
Product Packages
NDC Code 76351-100-01
Package Description: 51.03 g in 1 TUBE
Product Details
What is NDC 76351-100?
What are the uses for Tinted Moisturizer Spf-15?
Which are Tinted Moisturizer 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Tinted Moisturizer 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)
- CARBOMER 934 (UNII: Z135WT9208)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HYDROGENATED POLYBUTENE (370 MW) (UNII: V5H8103878)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2)
- SQUALANE (UNII: GW89575KF9)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- TROLAMINE (UNII: 9O3K93S3TK)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".