NDC | 51531-9004-7 |
Set ID | 121829b5-2a4a-473b-a949-a43186c97e8a |
Category | HUMAN OTC DRUG LABEL |
Packager | Mary Kay Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active Ingredients
- Purpose
- Uses
- Warnings
-
Directions
- apply liberally 15 minutes before sun exposure
- use a water-resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
- 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 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-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
-
Inactive ingredients
water/eau, glycerin, dicaprylyl carbonate, cetearyl alcohol, dimethicone, ammonium acryloyldimethyltaurate/VP copolymer, ceteareth-25, niacinamide, saccharomyces cerevisiae extract, opuntia ficus-indica fruit extract, tocopheryl acetate, bisabolol, oligopeptide-1, resveratrol, behenyl alcohol, jojoba esters, sucrose palmitate, disodium ethylene dicocamide PEG-15 disulfate, silica, hydroxypropyl cyclodextrin,
glyceryl linoleate, ethoxydiglycol, methyldihydrojasmonate, ethylene brassylate, tetramethyl acetyloctahydronaphthalenes,
ethyl linalool, isobutyl methyl tetrahydropyranol, methylenedioxyphenyl methylpropanal, phenylisohexanol, trimethylbenzenepropanol,
methyl benzodioxepinone, triethanolamine, disodium EDTA, sodium benzoate, ethylhexylglycerin, caprylhydroxamic acid, caprylyl glycol, propanediol, phenoxyethanol, iodopropynyl butylcarbamate. - Other information
- Questions or comments?
- Principal Display Panel - 48 g carton
-
INGREDIENTS AND APPEARANCE
MARY KAY TIMEWISE AGE MINIMIZE 3D DAY CREAM SPF 30 BROAD SPECTRUM SUNSCREEN (NORMAL TO DRY SKIN)
avobenzone, homosalate, octisalate, octocrylene, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51531-9004 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 3 g in 100 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 4.5 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) CETEARETH-25 (UNII: 8FA93U5T67) NIACINAMIDE (UNII: 25X51I8RD4) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) PRICKLY PEAR FRUIT (UNII: 18V8PAQ629) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) LEVOMENOL (UNII: 24WE03BX2T) RESVERATROL (UNII: Q369O8926L) DOCOSANOL (UNII: 9G1OE216XY) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) SUCROSE PALMITATE (UNII: 3OSQ643ZK5) DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYDROXYPROPYL .ALPHA.-CYCLODEXTRIN (UNII: ZFR0T80O4Y) GLYCERYL MONOLINOLEATE (UNII: 4763AXI84L) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES (UNII: 2JU6ZH6GRE) ETHYL LINALOOL (UNII: SF2JS9GF5T) 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F) 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA) PHENYLISOHEXANOL (UNII: M56178H183) TRIMETHYLBENZENEPROPANOL (UNII: 7S411YY2VY) METHYL BENZODIOXEPINONE (UNII: 0NQ136C313) TROLAMINE (UNII: 9O3K93S3TK) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM BENZOATE (UNII: OJ245FE5EU) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PROPANEDIOL (UNII: 5965N8W85T) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51531-9004-7 1 in 1 CARTON 05/16/2018 1 48 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:51531-9004-3 9 g in 1 TUBE; Type 0: Not a Combination Product 05/16/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 05/16/2018 Labeler - Mary Kay Inc. (049994452) Establishment Name Address ID/FEI Business Operations Englewood Lab Inc. 080987545 manufacture(51531-9004) Establishment Name Address ID/FEI Business Operations Mary Kay Inc. 103978839 manufacture(51531-9004)