NDC 11489-064 No7 Lifting And Firming Day Sunscreen Spf 8
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11489 - Bcm Ltd
- 11489-064 - No7 Lifting And Firming Day Sunscreen Spf 8
Product Packages
NDC Code 11489-064-01
Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR
Product Details
What is NDC 11489-064?
What are the uses for No7 Lifting And Firming Day Sunscreen Spf 8?
Which are No7 Lifting And Firming Day Sunscreen Spf 8 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are No7 Lifting And Firming Day Sunscreen Spf 8 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- ETHYLPARABEN (UNII: 14255EXE39)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
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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".