Label: NO7 PROTECT AND PERFECT INTENSE ADVANCED DAY CREAM SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, octocrylene, octisalate cream
- NDC Code(s): 11489-173-01
- 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 June 24, 2020
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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
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Inactive ingredients
Aqua (Water), C12-15 alkyl benzoate, Glycerin, Tribehenin, Alcohol denat., Aluminum starch octenylsuccinate, Dimethicone, Cetearyl glucoside, Butyrospermum parkii (Shea) butter, Butylene glycol, Ammonium acryloydimethyltaurate/VP copolymer, Phenoxyethanol, Potassium cetyl phosphate, Methylparaben, Dimethiconol, Parfum (Fragrance), Propylene glycol, Xanthan gum, Ascorbyl glucoside, Sodium hyaluronate, Tocopheryl acetate, Ethylparaben, Dipropylene glycol, Retinyl palmitate, Simethicone, Hydolyzed rice protein, Tetrasodium EDTA, Sorbitan laurate, Panax gingseng root extract, T-butyl alcohol, Carbomer, Dimethylmethoxy chromanol, Medicago sativa (Alfalfa) extract, Polyosorbate 20, Potassium hydroxide, Hydroxyethylcelulose, Acetyl dipeptide-1 cetyl ester, Morus alba leaf extract, Sodium benzoate, Tocopherol, Ethylhexylglycerin, Palmitoyl tripeptide-1, Palmitoyl tetrapeptide-7.
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INGREDIENTS AND APPEARANCE
NO7 PROTECT AND PERFECT INTENSE ADVANCED DAY CREAM SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, octocrylene, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11489-173 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) DIMETHICONE (UNII: 92RU3N3Y1O) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) TRIBEHENIN (UNII: 8OC9U7TQZ0) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) SHEA BUTTER (UNII: K49155WL9Y) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) METHYLPARABEN (UNII: A2I8C7HI9T) DIMETHICONOL (40 CST) (UNII: 343C7U75XW) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIPROPYLENE GLYCOL (UNII: E107L85C40) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLPARABEN (UNII: 14255EXE39) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) EDETATE SODIUM (UNII: MP1J8420LU) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) POLYSORBATE 20 (UNII: 7T1F30V5YH) DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TOCOPHEROL (UNII: R0ZB2556P8) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) MORUS ALBA LEAF (UNII: M8YIA49Q2P) SILICON (UNII: Z4152N8IUI) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) SODIUM BENZOATE (UNII: OJ245FE5EU) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) ALCOHOL (UNII: 3K9958V90M) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) ALFALFA SEED (UNII: 67PHZ58858) 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:11489-173-01 1 in 1 CARTON 06/24/2020 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 06/24/2020 Labeler - BCM Ltd (230780322) Registrant - The Boots Company PLC (218622660) Establishment Name Address ID/FEI Business Operations BCM Ltd 230780322 manufacture(11489-173) , analysis(11489-173)