NDC 61601-1239 Eve Lom Radiant Glow Cream Foundation Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61601 - Space Brands Limited
- 61601-1239 - Eve Lom Radiant Glow Cream Foundation Broad Spectrum Spf 30 Sunscreen
Product Characteristics
BROWN (C48332 - ECRU)
BROWN (C48332 - ALMOND)
BROWN (C48332 - HONEY)
WHITE (C48325 - CREAM)
ORANGE (C48331 - AMBER)
BROWN (C48332 - BAMBOO)
Product Packages
NDC Code 61601-1239-2
Package Description: 1 CONTAINER in 1 CARTON / 10 g in 1 CONTAINER
Product Details
What is NDC 61601-1239?
What are the uses for Eve Lom Radiant Glow Cream Foundation Broad Spectrum Spf 30 Sunscreen?
Which are Eve Lom Radiant Glow Cream Foundation Broad Spectrum Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Eve Lom Radiant Glow Cream Foundation Broad Spectrum Spf 30 Sunscreen 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:
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- MICA (UNII: V8A1AW0880)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYDROGENATED PALM KERNEL GLYCERIDES (UNII: UM8Y22J4JW)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SOYBEAN OIL (UNII: 241ATL177A)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOCOPHEROL (UNII: R0ZB2556P8)
* 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".