NDC 62032-115 Condition And Enhance Blender Skin Lightener And Blending
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62032 - Omp, Inc.
- 62032-115 - Condition And Enhance Blender
Product Packages
NDC Code 62032-115-10
Package Description: 28.5 g in 1 BOTTLE, PLASTIC
NDC Code 62032-115-36
Package Description: 57 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62032-115?
What are the uses for Condition And Enhance Blender Skin Lightener And Blending?
Which are Condition And Enhance Blender Skin Lightener And Blending UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Condition And Enhance Blender Skin Lightener And Blending 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:
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID (UNII: 33X04XA5AT)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- WATER (UNII: 059QF0KO0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERETH-26 (UNII: NNE56F2N14)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
What is the NDC to RxNorm Crosswalk for Condition And Enhance Blender Skin Lightener And Blending?
- RxCUI: 197795 - hydroquinone 4 % Topical Cream
- RxCUI: 197795 - hydroquinone 40 MG/ML Topical Cream
* 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".