PERFECTINT POWDER SPF 40 ALL SHADES- zinc oxide powder

PerfecTint Powder SPF 40 by

Drug Labeling and Warnings

PerfecTint Powder SPF 40 by is a Otc medication manufactured, distributed, or labeled by Science of Skincare, West Coast Cosmetics. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 25%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Apply liberally 15 minutes before sun exposure

WARNINGS

For external use only

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

When using this product keep out of eyes.

Rinse with water to remove.

STOP USE

Stop use and ask a doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

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 increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including:

limit time in the sun, especially from 10am - 2pm.

wear long-sleeve shirts, pants, hats, and sunglasses

Children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

QUESTIONS

Call Customer Care at (888)-804-4447

INACTIVE INGREDIENT

Mica, Dimethicone/Vinyl Dimethicone Crosspolymer, Calcium Sodium Borosilicate, Hydroxyapatite, Methyl Methacrylate Crosspolymer, Sodium Anisate, Lycopodium Clavatum Extract, Imperata Cylindrica Root Extract, Capryloyl Glycine, Glycerin, Triethoxycaprylylsiliane, Ironxe Oxides(CI 77491*, CI 77499*, CI77492*). *may contain one or more of these ingredients

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERFECTINT POWDER SPF 40  ALL SHADES
zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69219-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
MICA (UNII: V8A1AW0880)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
SODIUM ANISATE (UNII: F9WFJ28MV9)
LYCOPODIUM CLAVATUM WHOLE (UNII: 005ICF6L27)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
GLYCERIN (UNII: PDC6A3C0OX)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69219-111-01	3.5 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/19/2023
2	NDC: 69219-111-11	1 in 1 BOX	12/19/2023
2	NDC: 69219-111-01	3.5 g in 1 BOTTLE, PLASTIC; 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	12/19/2023

Labeler - Science of Skincare (006251958)