NDC 10967-669 Ceramide Premiere Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 10967-669?
What are the uses for Ceramide Premiere Broad Spectrum Spf 30?
Which are Ceramide Premiere Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Ceramide Premiere Broad Spectrum Spf 30 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:
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CERAMIDE 1 (UNII: 5THT33P7X7)
- FUCUS SERRATUS (UNII: V8K40WNW5B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- AMINO ACIDS, SOY (UNII: NWB9514AZM)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETIC ACID (UNII: 9G34HU7RV0)
- MICA (UNII: V8A1AW0880)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- CERAMIDE 6 II (UNII: F1X8L2B00J)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PEG-8 LAURATE (UNII: 762O8IWA10)
- TRAMIPROSATE (UNII: 5K8EAX0G53)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- AMINOPROPYL DIMETHICONE (1000 MPA.S) (UNII: P4P48I53XH)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DOCOSANOL (UNII: 9G1OE216XY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DESMENINOL CALCIUM (UNII: 1VK0YS654L)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- CERAMIDE 3 (UNII: 4370DF050B)
- YEAST (UNII: 3NY3SM6B8U)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".