NDC 62032-107 Obagi-c Rx System C-sunguard Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62032 - Omp, Inc.
- 62032-107 - Obagi-c Rx System C-sunguard
Product Characteristics
Product Packages
NDC Code 62032-107-90
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 90 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62032-107?
What are the uses for Obagi-c Rx System C-sunguard Spf 30?
Which are Obagi-c Rx System C-sunguard Spf 30 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)
Which are Obagi-c Rx System C-sunguard 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:
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LAURETH-7 (UNII: Z95S6G8201)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- 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)
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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".