NDC 62032-528 Obagi Medical - Nu-derm System - Normal To Dry - Skin Transformation Trial Kit
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62032-528?
What are the uses for Obagi Medical - Nu-derm System - Normal To Dry - Skin Transformation Trial Kit?
Which are Obagi Medical - Nu-derm System - Normal To Dry - Skin Transformation Trial Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Obagi Medical - Nu-derm System - Normal To Dry - Skin Transformation Trial Kit 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:
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM DIHYDROXYCETYL PHOSPHATE (UNII: YWI33EV595)
- SQUALANE (UNII: GW89575KF9)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- TROPOLONE (UNII: 7L6DL16P1T)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- LACTIC ACID (UNII: 33X04XA5AT)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
What is the NDC to RxNorm Crosswalk for Obagi Medical - Nu-derm System - Normal To Dry - Skin Transformation Trial Kit?
- RxCUI: 197795 - hydroquinone 4 % Topical Cream
- RxCUI: 197795 - hydroquinone 40 MG/ML Topical Cream
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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".