KISS MY FACE BARE NAKED 30 MINERAL SUNSCREEN- titanium dioxide spray

Kiss My Face Bare Naked 30 Mineral Sunscreen by

Drug Labeling and Warnings

Kiss My Face Bare Naked 30 Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by Windmill Health Products, LLC, Bell International Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Titanium dioxide 7.8%

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

• Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120°F.
• 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 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.
• Hold 4 to 6 inches away from body when spraying.
• Do not spray directly on face and avoid breathing mist. Spray on hand and apply to face.
• Do not apply in windy conditions.
• Use in well-ventilated areas and avoid inhalation.
• 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.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Alumina, Bentonite, Butyloctyl Salicylate, Caprylhydroxamic Acid, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Alcohol , Coco Glucoside, Cucumis Sativus (Cucumber) Fruit Extract, Ethylhexylglycerin, Fragrance (Parfum)1, Ginkgo Biloba Leaf Extract, Glycerin, Heptyl Undecylenate, Impatiens Balsamina (Garden Balsam) Leaf Extract, Methyl Dihydroabietate, Persea Gratissima (Avocado) Fruit Extract, Silica, Tocopherol, Water (Aqua)

1 Natural fragrance

Other Information

• Protect this product from excessive heat and direct sun.

Questions?

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

PRINCIPAL DISPLAY PANEL - 177 ml Can Label

KISS
MY
FACE®

30
bare naked®

mineral sunscreen
lightweight & ultra sheer**

broad spectrum SPF30
water resistant (80 minutes)

hydrates & protects

aloe vera
ginkgo biloba

REEF FRIENDLY*

6 fl oz (177 ml)

INGREDIENTS AND APPEARANCE

KISS MY FACE BARE NAKED 30 MINERAL SUNSCREEN 
titanium dioxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74154-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium dioxide (UNII: 15FIX9V2JP) (Titanium dioxide - UNII:15FIX9V2JP)	Titanium dioxide	0.078 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALUMINUM OXIDE (UNII: LMI26O6933)
Bentonite (UNII: A3N5ZCN45C)
Butyloctyl Salicylate (UNII: 2EH13UN8D3)
Caprylhydroxamic Acid (UNII: UPY805K99W)
Caprylyl Glycol (UNII: 00YIU5438U)
SAFFLOWER OIL (UNII: 65UEH262IS)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
Coco Glucoside (UNII: ICS790225B)
CUCUMBER (UNII: YY7C30VXJT)
Ethylhexylglycerin (UNII: 147D247K3P)
GINKGO (UNII: 19FUJ2C58T)
Glycerin (UNII: PDC6A3C0OX)
Heptyl Undecylenate (UNII: W77QUB6GXO)
IMPATIENS BALSAMINA LEAF (UNII: LH9E1X602V)
Methyl Dihydroabietate (UNII: 7666FJ0J9F)
AVOCADO (UNII: SDS87L369F)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74154-012-06	177 mL in 1 CAN; Type 0: Not a Combination Product	02/18/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	02/18/2022

Labeler - Windmill Health Products, LLC (831136267)

Establishment
Name	Address	ID/FEI	Business Operations
Bell International Laboratories		967781555	MANUFACTURE(74154-012)