MARY KAY TIMEWISE AGE MINIMIZE 3D DAY CREAM SPF 30 BROAD SPECTRUM SUNSCREEN (COMBO TO OILY SKIN)- avobenzone, homosalate, octisalate, octocrylene, oxybenzone cream 
Mary Kay Inc.

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.

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Mary Kay TimeWise Age Minimize 3D Day Cream SPF 30 (Combo/Oily)

Drug Facts

Active Ingredients

Avobenzone 3%

Homosalate 9%

Octisalate 4.5%

Octocrylene 3%

Oxybenzone 4.5%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water/eau, glycerin, dicaprylyl carbonate, dimethicone, ammonium acryloyldimethyltaurate/VP copolymer, cetearyl alcohol, ceteareth-25, niacinamide, opuntia ficus-indica fruit extract, saccharomyces cerevisiae extract, tocopheryl acetate, oligopeptide-1, resveratrol, sucrose 
palmitate, bisabolol, silica, disodium ethylene dicocamide PEG-15 disulfate, hydroxypropyl cyclodextrin, glyceryl linoleate, ethoxydiglycol, methyldihydrojasmonate, ethylene brassylate, tetramethyl acetyloctahydronaphthalenes, ethyl linalool, isobutyl methyl tetrahydropyranol,  methylenedioxyphenyl methylpropanal, phenylisohexanol, trimethylbenzenepropanol, methyl benzodioxepinone, triethanolamine, 
sodium benzoate, disodium EDTA, caprylhydroxamic acid, phenoxyethanol, ethylhexylglycerin, propanediol, caprylyl glycol, iodopropynyl  butylcarbamate.

Other information

Questions or comments?

Call toll free 1-800-627-9529

Principal Display Panel - 48 g carton

Mary Kay

timewise age minimize 3D day cream

spf 30 broad spectrum suncreen

1.7 OZ. NET WT. / 48 g

image of carton

MARY KAY TIMEWISE AGE MINIMIZE 3D DAY CREAM SPF 30 BROAD SPECTRUM SUNSCREEN (COMBO TO OILY SKIN) 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-9005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE3 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE4.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETEARETH-25 (UNII: 8FA93U5T67)  
NIACINAMIDE (UNII: 25X51I8RD4)  
PRICKLY PEAR FRUIT (UNII: 18V8PAQ629)  
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
RESVERATROL (UNII: Q369O8926L)  
SUCROSE PALMITATE (UNII: 3OSQ643ZK5)  
LEVOMENOL (UNII: 24WE03BX2T)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)  
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)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PROPANEDIOL (UNII: 5965N8W85T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51531-9005-71 in 1 CARTON05/16/2018
148 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:51531-9005-39 g in 1 TUBE; Type 0: Not a Combination Product05/16/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02005/16/2018
Labeler - Mary Kay Inc. (049994452)
Establishment
NameAddressID/FEIBusiness Operations
Englewood Lab Inc.172198223manufacture(51531-9005)
Establishment
NameAddressID/FEIBusiness Operations
Mary Kay Inc.103978839manufacture(51531-9005)

Revised: 7/2023
Document Id: 013f12a8-05ef-73e7-e063-6294a90a4f5b
Set id: 5ac23cf9-9954-4843-8343-fdb41d48af2d
Version: 7
Effective Time: 20230724
 
Mary Kay Inc.