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

Kiss My Face Purely Mineral Face Factor 50 Sunscreen SPF 50 by

Drug Labeling and Warnings

Kiss My Face Purely Mineral Face Factor 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
• retains SPF after 80 minutes of swimming or sweating
• 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

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 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 minutes before sun exposure and as needed.
• Children under 6 months of age: ask a doctor.
• Reapply:
• after 80 minutes 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 the risk, regularly use a sunscreen with broad spectrum SPF 15 or higher and other sun protection measures including:
•  Limit time in sun, especially from 10a.m.- 2 p.m.
•  Wear long-sleeved shirts, pants, hats and sunglasses.

Other Information

•  Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

Acetic Acid, Acetyl Hexapeptide-8, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Ascorbic Acid, Butylene Glycol, Butylene Glycol, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Calendula Officinalis Extract, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Carbomer, Cetearyl Alcohol, Cetearyl Glucoside, Chamomilla Recutlta (Matricaria) Flower Extract, Citric Acid, Citrullus Lanatus (Watermelon) Fruit Extract, Cocos Nucifera (Coconut) Oil, Decyl Glucoside, Dodecane, Glycerin, Glyceryl Caprylate, Glyceryl Stearate SE, Glyceryl Undecylenate, Helianthus Annuus (Sunflower) Seed Oil, Laminaria Digitata Extract, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Persea Gratissima (Avacado) Oil, Polyhydroxvstearic Acid, Polysorbate 20, Potassium Sorbate, Propanediol, Sodium Hyaluronate, Sodium Stearoyl Glutamate, Stearic Acid, Sucrose, Tapioca Starch, Tocopherol, Tridecyl Salicylate, Water (Aqua), Xanthan Gum, Xanthophylls

Questions?

(800) 822-4320 

Package labelling:

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74154-902
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
ACETIC ACID (UNII: Q40Q9N063P)
ACETYL HEXAPEPTIDE-8 AMIDE (UNII: L4EL31FWIL)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
ARGAN OIL (UNII: 4V59G5UW9X)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SHEA BUTTER (UNII: K49155WL9Y)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CHAMOMILE (UNII: FGL3685T2X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATERMELON (UNII: 231473QB6R)
COCONUT (UNII: 3RT3536DHY)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DODECANE (UNII: 11A386X1QH)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
SUNFLOWER OIL (UNII: 3W1JG795YI)
LAMINARIA DIGITATA (UNII: 15E7C67EE8)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
AVOCADO (UNII: SDS87L369F)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPANEDIOL (UNII: 5965N8W85T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
STEARIC ACID (UNII: 4ELV7Z65AP)
SUCROSE (UNII: C151H8M554)
STARCH, TAPIOCA (UNII: 24SC3U704I)
TOCOPHEROL (UNII: R0ZB2556P8)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74154-902-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/13/2026

Labeler - Windmill Health Products, LLC (831136267)

Registrant - Pure Source, LLC (080354456)