Label: NO7 LIFT AND LUMINATE TRIPLE ACTION DAY CREAM SPF 30- avobenzone,octisalate, octocrylene cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 11489-148-01 - Packager: BCM Ltd
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 20, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Carton Active Ingredients Section
- Uses
- Warnings
- Ask a doctor
- Keep out of reach of children
-
Directions
Directions
apply liberally 15 minutes before sun exposure.
reapply at least every 2 hours.
use a water resistant sunscreen if swimming or sweating.
children under 6 months of age: Ask a doctor.
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
Limit time in the sun, especially from 10 a.m - 2 p.m.
wear long-sleeved shirts, pants, hats and sunglasses
- Storage
-
Inactive ingredients
Aqua (Water), C12-15 alkyl benzoate, Glycerin, Tribehenin, Alcohol denat., Butylene glycol, Aluminum starch octenylsuccinate, Dimethicone, Mica, Cetearyl alcohol, Butyrospermum parkii (Shea) butter, Cetearyl glucoside, Ammonium acryloyldimethyltaurate/VP copolymer, Phenoxyethanol, Potassium cetyl phosphate, Methylparaben, Dimethiconol, Ascorbyl glucoside, Parfum (Fragrance), Propylene glycol, Xanthan gum, Ethylparaben, Pentylene glycol, Sodium hyaluronate, Tocopheryl acetate, Hibiscus abelmoschus extract, Retinyl palmitate, Simethicone, Phyllanthus emblica fruit extract, Hydrolyzed rice protein, Tetrasodium EDTA, Sorbitan laurate, T-butyl alcohol, Potassium hydroxide, Carbomer, Panax ginseng root extract, Dipropylene glycol, Dimethylmoethoxy chromanol, Polysorbate 20, Hydroxyethylcellulose, Acetyl dipeptide-1 cetyl ester, Morus alba leaf extract, Sodium benzoate, Tocopherol, Palmitoyl tripeptide-1, Palmitoyl tetrapeptide-7, CI77891 (Titanium dioxide).
- INFORMATION FOR PATIENTS
- Description
- carton
-
INGREDIENTS AND APPEARANCE
NO7 LIFT AND LUMINATE TRIPLE ACTION DAY CREAM SPF 30
avobenzone,octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11489-148 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 0.75 g in 25 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 1.875 g in 25 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 1.25 g in 25 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) DIMETHICONE (UNII: 92RU3N3Y1O) MICA (UNII: V8A1AW0880) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) TRIBEHENIN (UNII: 8OC9U7TQZ0) PENTYLENE GLYCOL (UNII: 50C1307PZG) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SHEA BUTTER (UNII: K49155WL9Y) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) METHYLPARABEN (UNII: A2I8C7HI9T) DIMETHICONOL (40 CST) (UNII: 343C7U75XW) ETHYLPARABEN (UNII: 14255EXE39) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) EDETATE SODIUM (UNII: MP1J8420LU) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYSORBATE 20 (UNII: 7T1F30V5YH) DIPROPYLENE GLYCOL (UNII: E107L85C40) DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) TOCOPHEROL (UNII: R0ZB2556P8) MORUS ALBA LEAF (UNII: M8YIA49Q2P) SODIUM BENZOATE (UNII: OJ245FE5EU) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ALCOHOL (UNII: 3K9958V90M) SILICON (UNII: Z4152N8IUI) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR) ABELMOSCHUS MOSCHATUS WHOLE (UNII: M7QAW6696G) ASIAN GINSENG (UNII: CUQ3A77YXI) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11489-148-01 1 in 1 CARTON 08/20/2019 1 25 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/17/2019 Labeler - BCM Ltd (230780322) Registrant - The Boots Company PLC (218622660) Establishment Name Address ID/FEI Business Operations BCM Ltd 230780322 manufacture(11489-148) , analysis(11489-148)