KISS MY FACE PURELY MINERAL DAILY 50 SUNSCREEN SPF 50- zinc oxide lotion

Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50 by

Drug Labeling and Warnings

Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50 by is a Otc medication manufactured, distributed, or labeled by Windmill Health Products, LLC, Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Zinc Oxide - 17.50%

Purpose

Sunscreen

Uses:

• Helps prevent sunburn
• Higher SPF gives more sunburn protection
• If used as directed with other sun protection measures (see Directions), decreases risk of skin cancer and early skin aging caused by the sun.

Warnings:

For external use only
Not intended for ingestion.

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 skin rash or irritation develops and lasts.

Keep out of reach of children.

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

If pregnant or breast-feeding,

ask a health professional before use.

Directions:

• Apply liberally 15 minute before sun exposure.
• Reapply:
• after 80 minutes of swimming or sweating,
• immediately after towel drying and at least every 2 hours.
• Children under 6 months: ask a doctor. Sun Protection Measures:Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with Broad Spectrum SPF 15 or higher and other sun protection measures including:
•  Limit time in sun, especially from 10am to 2pm.
•  Wear long-sleeved shirts, pants, hats and sunglasses.

Other Information

•  Protect this product from excessive heat and direct sun.

Ingredients:

Aloe Barbadensis Leaf Juice, Ascorbic Acid, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetearyl Glucoside, Chamomilla Recutlta (Matricaria) Flower Extract, Citric Acid, Cocos Nucifera (Coconut) Oil, Daucus Carota Sativa (Carrot) Seed Extract, Decyl Glucoside, Dodecane, Glycerin, Glyceryl Caprylate, Glyceryl Stearate SE, Glyceryl Undecylenate, Helianthus Annuus (Sunflower) Seed Oil, Laminaria Digitata Extract, Persea Gratissima (Avocado) Oil, Polyhydroxvstearic Acid, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Stearoyl Glutamate, Stearic Acid, Sucrose, Tapioca Starch, Tocopherol, Tridecyl Salicylate, Water (Aqua), Xanthan Gum, Xanthophylls

Questions?

Call 800-822-4320 Or visit www.kissmyface.comlnactive

Package labelling:

INGREDIENTS AND APPEARANCE

KISS MY FACE PURELY MINERAL DAILY 50 SUNSCREEN SPF 50 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74154-903
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	175 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCONUT (UNII: 3RT3536DHY)
DAUCUS CAROTA SUBSP. SATIVUS SEED (UNII: 9M6AAX381U)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DODECANE (UNII: 11A386X1QH)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
LAMINARIA DIGITATA (UNII: 15E7C67EE8)
AVOCADO (UNII: SDS87L369F)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74154-903-00	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/04/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/04/2026

Labeler - Windmill Health Products, LLC (831136267)

Registrant - Pure Source, LLC (080354456)