Label: NO7 LIFT AND LUMINATE DAY SUNSCREEN BROAD SPECTRUM SPF 15- avobenzone, octinoxate, octocrylene cream
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Contains inactivated NDC Code(s)
NDC Code(s): 11489-075-01 - Packager: BCM Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 May 1, 2012
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS AND PRECAUTIONS
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
Directons
Apply liberally 15 minutes before sun exposure
Use a water resistant sunscreen if swimming or sweating
Reapply at least every 2 hours
Chidren 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 10a,m - 2p.m
wear long-sleeved shirts, pants, hat and sunglasses
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive Ingredients
Aqua (water), Glycerin, C12-15 alkyl benzoate, Butyrospermum parkii (shea) butter, Butylene glycol, Cetearyl glucoside, C18-36 acid glycol ester, Dimethicone, Mica, Cetearyl alcohol, Cyclopentasiloxane, Ammonium acryloyldimethyltaurate/VP coplymer, Phenoxyethanol, Cyclohexasiloxane, Potassium cetyl phosphate, Dipalmitoyl hydroxyproline, Xanthan gum, Methylparaben, Sodium ascorbyl phosphate, Dimethiconol, Parfum (Fragrance), Ethylparaben, Dipropylene glycol, Tetrasodium EDTA, Citric acid, T-butyl alcohol, Lupinus albus seed extract, Carbomer, Polysorbate 20, Haematococcus Pluvialis powder, BHT, Polyglucuronic acid, Potassium sorbate, Simethicone, Butylparaben, Propylparaben, Isobutylparaben, Palmitoyl oligopeptide, Palmitoyl tetrapeptide-7, Biotin, CI 77891 (Titanium dioxide)
- QUESTIONS
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DESCRIPTION
Firm, lift and brighten your skin with this multitasking day cream. Formulated to give your skin an instant brightening boost and healthy glow, it then works day by day to chase away the signs of ageing. Visibly reduces the appearance of lines and wrinkles, evens skin tone and lifts and firms for younger more luminous looking skin in 4 weeks.
- INFORMATION FOR PATIENTS
- INSTRUCTIONS FOR USE
- ACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- INFORMATION FOR PATIENTS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO7 LIFT AND LUMINATE DAY SUNSCREEN BROAD SPECTRUM SPF 15
avobenzone, octinoxate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11489-075 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 1.5 mL in 50 mL Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 2.5 mL in 50 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 0.5 mL in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SHEA BUTTER (UNII: K49155WL9Y) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) Dimethicone (UNII: 92RU3N3Y1O) mica (UNII: V8A1AW0880) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) Phenoxyethanol (UNII: HIE492ZZ3T) CYCLOMETHICONE 6 (UNII: XHK3U310BA) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H) XANTHAN GUM (UNII: TTV12P4NEE) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) ETHYLPARABEN (UNII: 14255EXE39) DIPROPYLENE GLYCOL (UNII: E107L85C40) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) LUPINUS ALBUS SEED (UNII: 24GB753W3B) POLYSORBATE 20 (UNII: 7T1F30V5YH) HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) BUTYLPARABEN (UNII: 3QPI1U3FV8) PROPYLPARABEN (UNII: Z8IX2SC1OH) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) biotin (UNII: 6SO6U10H04) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11489-075-01 1 in 1 CARTON 1 50 mL in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/01/2012 Labeler - BCM Ltd (230780322) Registrant - The Boots Company PLC (218622660) Establishment Name Address ID/FEI Business Operations BCM Ltd 230780322 manufacture, analysis