NDC 61589-3811 No7 Lifting And Firming Foundation Sunscreen Spf 15 Nude 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61589 - Bcm Cosmetique Sas
- 61589-3811 - No7 Lifting And Firming Foundation Sunscreen Spf 15 Nude
Product Packages
NDC Code 61589-3811-1
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 61589-3811?
What are the uses for No7 Lifting And Firming Foundation Sunscreen Spf 15 Nude 15?
Which are No7 Lifting And Firming Foundation Sunscreen Spf 15 Nude 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are No7 Lifting And Firming Foundation Sunscreen Spf 15 Nude 15 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 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- OCTYLTRIETHOXYSILANE (UNII: LDC331P08E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".