NDC 58633-233 Cc Spf 18 Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58633 - Dr. Dennis Gross Skincare, Llc
- 58633-233 - Cc Spf 18
Product Characteristics
Product Packages
NDC Code 58633-233-10
Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE
NDC Code 58633-233-60
Package Description: 7 mL in 1 TUBE
Product Details
What is NDC 58633-233?
What are the uses for Cc Spf 18 Medium?
Which are Cc Spf 18 Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Cc Spf 18 Medium 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)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- EMU OIL (UNII: 344821WD61)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM ASCORBATE (UNII: S033EH8359)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
* 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".