Mary Kay Suncare Sunscreen Broad Spectrum SPF 50

Manufacturer
Mary Kay Inc.
Effective date
2021-11-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:29:29

Label at a glance#

ProductMary Kay Suncare Sunscreen Broad Spectrum SPF 50
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 •reapply: •    after 80 munutes of swimming or sweating •    immediately after towel drying •    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: •    ...

Storage and handling

•protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 4.5%

Octocrylene 5.5%

Oxybenzone 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
•reapply:
•    after 80 munutes of swimming or sweating
•    immediately after towel drying
•    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

acrylates/C12-22 alkyl methacrylate copolymer, acrylates/dimethicone copolymer,

ammonium acryloyldimethyltaurate/vp copolymer, ammonium hydroxide, behenyl alcohol,

butylene glycol, butyloctyl salicylate, caprylyl glycol,

cetearyl alcohol, ceteth-20 phosphate, cyclamen

aldehyde, dicetyl phosphate, dimethicone, disodium

EDTA, ethyl linalool, ethylene brassylate, ethylhexyl

methoxycrylene, euterpe oleracea

fruit extract, glycerin, isobutyl methyl

tetrahydropyranol, methyl trimethicone, methylenedioxyphenyl

methylpropanal,  pentylene glycol, phenoxyethanol, phenylisohexanol,

propylene glycol, silica, sorbic acid,

styrene/acrylates copolymer, tocopheryl acetate,

triethanolamine, trimethylsiloxysilicate, vp/eicosene

copolymer, water, xanthan gum

Other information

STORAGE AND HANDLING SECTION

•protect this product from excessive heat and direct sun

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-627-9529

Principal Display Panel - 118 mL carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mary Kay

suncare

sunscreen

broad spectrum spf 50

protector solar

con amplia proteccion solar fps 50

water resistant

(80 minutes)

a prueba de agua

(80 minutos)

4 FL. OZ. / 118 mL

image of cartonimage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51531-3276-42020-07-22C16284748780-1ab0e2407-299b-f274-e053-dbdaa90a6471Mary Kay Suncare Sunscreen SPF 50 (reformulation) Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51531-327651531-3276-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
297a5495-6a55-857c-e063-6394a90a531e91d16ee2-aefe-44f8-a58a-3cfd19a543f92024-12-17WarningsExact identifier
spl set id: 91d16ee2-aefe-44f8-a58a-3cfd19a543f9

Reported adverse events (FAERS/openFDA)#

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