NDC | 59779-777-01 |
Set ID | cca5d399-5017-4b8d-8a19-3f6370664c18 |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS Pharmacy, Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active Ingredients
- Use
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- Use water resistant sunscreen if swimming or sweathing
- Reapply at least every 2 hours
- Children under 6 months: ask a doctor
- Sun Protection Measures: Spending time in the sun decreases risk of skin cancer and early again. To decrease this risk, regulaory 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 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses.
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Inactive Ingredients
Water (Aqua, Eau), Octyldodecyl Neopentanoate, C12-15 Alkyl Benzoate, Butylene Glycol, Mica, Titanium Dioxide (CI 77891), Glycerin, Simmondsia Chinensis Seed Oil, Butyrospermum Parkii (Shea) Butter, Hexapeptide-33, Stearic Acid, Behenyl Alcohol, Glyceryl Stearate, Lecithin,Myristyl Alcohol, Lauryl Alcohol, Cetyl Alcohol, Palmitic Acid, Cetearyl Alcohol, Coco-Glucoside, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Prunus Armeniaca Kernel Oil, Carica Papaya Fruit Extract, Cymbopogon Schoenanthus Extract, Aesculus Hippocastanum Seed Extract, Aloe Barbadensis Leaf Extract, Polysorbate 20, Sorbitan Laurate, Propylene Glycol Stearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Sodium Hydroxide, Propylene Glycol Laurate, Ethylhexylglycerin, Disodium Edta, Phenoxyethanol, o-Cymen-5-Ol, Fragrance (Parfum), Benzyl Alcohol, Benzyl Salicylate, Butylphenyl Methylpropional, d-Limonene
- Other Information
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
NUANCE SALMA HAYEK RENEWED RADIANCE MOISTURIZING DAY CREAM BROAD SPECTRUM SPF 30 SUNSCREEN
nuance salma hayek renewed radiance moisturizing day cream broad spectrum spf 30 sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-777 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) GLYCERIN (UNII: PDC6A3C0OX) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) SHEA BUTTER (UNII: K49155WL9Y) STEARIC ACID (UNII: 4ELV7Z65AP) BEHENYL BENZOATE (UNII: DQG8119XKJ) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) MYRISTYL ALCOHOL (UNII: V42034O9PU) LAURYL ALCOHOL (UNII: 178A96NLP2) CETYL ALCOHOL (UNII: 936JST6JCN) PALMITIC ACID (UNII: 2V16EO95H1) COCO GLUCOSIDE (UNII: ICS790225B) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) PRUNUS ARMENIACA LEAF (UNII: 0X5YG5R83N) CARICA PAPAYA LEAF (UNII: 66J7636Z2I) CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO) AESCULUS HIPPOCASTANUM LEAF (UNII: Z49U891FNQ) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITAN OLIVATE (UNII: MDL271E3GR) PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0) CARBOMER 940 (UNII: 4Q93RCW27E) SODIUM HYDRIDE (UNII: 23J3BHR95O) PROPYLENE GLYCOL LAURATES (UNII: 40KT317HGP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) PHENOXYETHANOL (UNII: HIE492ZZ3T) O-CYMEN-5-OL (UNII: H41B6Q1I9L) BENZYL ALCOHOL (UNII: LKG8494WBH) BENZYL SALICYLATE (UNII: WAO5MNK9TU) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-777-01 1 in 1 PACKAGE 01/18/2017 1 40 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 01/18/2017 Labeler - CVS Pharmacy, Inc (062312574)