NDC 68472-141 No7 Dual Action Tinted Moisturiser Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68472 - Boots Retail Usa Inc
- 68472-141 - No7 Dual Action Tinted Moisturiser Medium
Product Packages
NDC Code 68472-141-01
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Details
What is NDC 68472-141?
What are the uses for No7 Dual Action Tinted Moisturiser Medium?
Which are No7 Dual Action Tinted Moisturiser Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are No7 Dual Action Tinted Moisturiser Medium 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MICA (UNII: V8A1AW0880)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- ROSA MOSCHATA SEED OIL (UNII: T031ZE559T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLPARABEN (UNII: 14255EXE39)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- LAURETH-7 (UNII: Z95S6G8201)
- PHYLLANTHUS EMBLICA FRUIT JUICE (UNII: K8SGU56WPQ)
- CERAMIDE 3 (UNII: 4370DF050B)
- GINKGO BILOBA LEAF OIL (UNII: Y5967KO1JH)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
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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".