NDC 11489-102 No7 Early Defence Day Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11489 - Bcm Ltd
- 11489-102 - No7 Early Defence Day Cream
Product Characteristics
Product Packages
NDC Code 11489-102-01
Package Description: 1 JAR in 1 CARTON / 50 g in 1 JAR
Product Details
What is NDC 11489-102?
What are the uses for No7 Early Defence Day Cream?
Which are No7 Early Defence Day Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are No7 Early Defence Day Cream 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)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SHEA BUTTER (UNII: K49155WL9Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- MEDICAGO SATIVA LEAF (UNII: HY3L927V6M)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- MORUS ALBA LEAF (UNII: M8YIA49Q2P)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
* 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".