MARY KAY MINERAL FACIAL SUNSCREEN BROAD SPECTRUM SPF30- zinc oxide lotion

Mary Kay Mineral Facial Sunscreen Broad Spectrum SPF30 by

Drug Labeling and Warnings

Mary Kay Mineral Facial Sunscreen Broad Spectrum SPF30 by is a Otc medication manufactured, distributed, or labeled by Mary Kay Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 22.973%

Purpose

Sunscreen

Uses

• helps prevent sunburn

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

• 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

ascorbic acid, bisabolol, c12-15 alkyl
benzoate, caprylyl glycol, ceteareth-25,
cetearyl alcohol, chlorphenesin, citric acid,
dimethicone, disodium edta, disodium
ethylene dicocamide peg-15 disulfate,
glyceryl behenate/eicosadioate, glyceryl
stearate, hydrogen dimethicone,
hydroxyethyl acrylate/sodium
acryloyldimethyl taurate copolymer,
isononyl isononanoate, isopropyl myristate,
myrothamnus flabellifolia leaf/stem extract,
phenoxyethanol, polyhydroxystearic acid,
polysorbate 60, propanediol, propylene
carbonate, silica, sorbitan isostearate,
squalane, stearalkonium hectorite,
tocopheryl acetate, triethoxycaprylylsilane,
water/eau/aqua, xanthan gum.

Other information

• protect this product from excessive heat and direct sun

Questions or comments?

Questions? 1-800-627-9529

Principal Display Panel - 1.7 oz

Mary Kay

Mineral Facial Sunscreen

Broad Spectrum SPF 30

1.7 oz net wt/40 g

Mineral Sunscreen Carton

Mineral Sunscreen Tube

INGREDIENTS AND APPEARANCE

MARY KAY MINERAL FACIAL SUNSCREEN BROAD SPECTRUM SPF30 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51531-3253
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	22.973 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CHLORPHENESIN (UNII: I670DAL4SZ)
LEVOMENOL (UNII: 24WE03BX2T)
CETEARETH-25 (UNII: 8FA93U5T67)
SQUALANE (UNII: GW89575KF9)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5)
POLYSORBATE 60 (UNII: CAL22UVI4M)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PROPANEDIOL (UNII: 5965N8W85T)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51531-3253-7	1 in 1 CARTON	02/24/2024
1		48 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 Drug	M020	02/24/2024

Labeler - Mary Kay Inc. (049994452)

Establishment
Name	Address	ID/FEI	Business Operations
Mary Kay Inc.		103978839	manufacture(51531-3253)