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

Manufacturer
Mary Kay Inc. | Englewood Lab Inc.
Effective date
2023-07-24
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:28:04

Label at a glance#

ProductMary Kay TimeWise Age Minimize 3D Day Cream SPF 30 Broad Spectrum Sunscreen (Combo to Oily Skin)
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure9 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

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, es...

Storage and handling

protect this product from excessive heat and direct sun store above 32° F/0° C

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 9%

Octisalate 4.5%

Octocrylene 3%

Oxybenzone 4.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun
  • store above 32° F/0° C

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-627-9529

Principal Display Panel - 48 g carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mary Kay

timewise age minimize 3D day cream

spf 30 broad spectrum suncreen

1.7 OZ. NET WT. / 48 g

image of cartonimage of carton

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 44 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51531-900551531-9005-7, 51531-9005-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 42 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
297a30cb-46dd-fb2d-e063-6294a90a823a5ac23cf9-9954-4843-8343-fdb41d48af2d2024-12-17WarningsExact identifier
spl set id: 5ac23cf9-9954-4843-8343-fdb41d48af2d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.