Label: NO7 BEAUTIFUL SKIN DAY DRY VERY DRY SUNSCREEN BROAD SPECTRUM SPF 15- avobenzone, octisalate and octocrylene cream
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Contains inactivated NDC Code(s)
NDC Code(s): 11489-072-01 - 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 January 9, 2020
If you are a consumer or patient please visit this version.
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INACTIVE INGREDIENT
Inactive Ingredients
Aqua (water), Glycerin, C12-15 alkyl benzoate, Dimethicone, Cetearyl alcohol, Cetearyl glucoside, Aluminum starch octenylsuccinate, Tribehenin, Ammonium acryloyldimethyltaurate/VP copolymer, Phenoxyethanol, Tocopheryl acetate, Butyrospermum parkii (Shea) butter, Potassium cetyl phosphate, Parfum (Fragrance), Methylparaben, Sodium PCA, Xanthan gum, Ethylparaben, Sodium lauroyl lactylate, Ascorbyl glucoside, Tetrasodium EDTA, Magnesium PCA, Dipropylene glycol, T-butyl alcohol, Zinc PCA, Biosaccharide gum-1, Ceramide 3, Potassium hydroxide, Ceramide 6 II, Ceramide 1, Phytosphingosine, Cholesterol, Carbomer, Manganese PCA, Ethylhexylglycerin, Simethicone, Potassium sorbate
- QUESTIONS
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DESCRIPTION
A rich and intensive moisture cream to instantly nourish and provide hydration for 24 hours whilst leaving skin looking and feeling healthy and radiant.The protective power of SPF 15 and broad spectrum sunscreens give you advanced protection for the future and and help keep you looking as young as possible.
Hypo-allergenic: Because all skin can have sensitive moments all our products are hypo-allergenic, using ingredients we know and trust.
www.boots.com/no7
- DESCRIPTION
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS AND PRECAUTIONS
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
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INSTRUCTIONS FOR USE
Directions
Apply liberally 15 minutes before sun exposure
Use a water resistant sunscreen if swimming or sweating
Reapply at least every 2 hours
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 10a.m. - 2p.m.
wear long-sleeved shirts, pants, hat and sunglasses
- STORAGE AND HANDLING
- INSTRUCTIONS FOR USE
- WARNINGS
- ACTIVE INGREDIENT
- INFORMATION FOR PATIENTS
- Carton
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INGREDIENTS AND APPEARANCE
NO7 BEAUTIFUL SKIN DAY DRY VERY DRY SUNSCREEN BROAD SPECTRUM SPF 15
avobenzone, octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11489-072 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 1.5 mg in 50 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 1 mg in 50 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 2 mg in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Dimethicone (UNII: 92RU3N3Y1O) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) TRIBEHENIN (UNII: 8OC9U7TQZ0) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SHEA BUTTER (UNII: K49155WL9Y) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLPARABEN (UNII: 14255EXE39) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) EDETATE SODIUM (UNII: MP1J8420LU) MAGNESIUM PIDOLATE (UNII: V5PC588N7G) DIPROPYLENE GLYCOL (UNII: E107L85C40) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) ZINC PIDOLATE (UNII: C32PQ86DH4) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) CERAMIDE 3 (UNII: 4370DF050B) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) CERAMIDE 6 II (UNII: F1X8L2B00J) CERAMIDE 1 (UNII: 5THT33P7X7) CHOLESTEROL (UNII: 97C5T2UQ7J) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11489-072-01 1 in 1 CARTON 05/02/2012 1 50 mL in 1 JAR; 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 05/02/2012 Labeler - BCM Ltd (230780322) Registrant - The Boots Company PLC (218622660) Establishment Name Address ID/FEI Business Operations BCM Ltd 230780322 manufacture(11489-072) , analysis(11489-072)