SUPERGOOP GLOW SCREEN SPF 40 SHADE 2 GOLDEN HOUR- broad spectrum sunscreen cream

Supergoop Glow Screen SPF 40 by

Drug Labeling and Warnings

Supergoop Glow Screen SPF 40 by is a Otc medication manufactured, distributed, or labeled by Supergoop LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Active Ingredients Purpose Avobenzone 3% Sunscreen Homosalate 4% Sunscreen Octisalate 5% Sunscreen Octocrylene 8% Sunscreen

Purpose

Uses Helps prevent sunburn If used as directed with other sun protection measures (see Directions), decreases

the risk of skin cancer and early skin aging caused by the sun

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

Indications and Usage

Stop use and ask a doctor if rash occurs

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

Dosage and Administration

Apply generously and evenly 15 minutes before sun exposure
rRapply at least every 2 hours
Use a water resistant Sunscreen if swimming or sweating
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 value 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-sleeved shirts, pants, hats, and sun glasses
Children under 6 months: Ask a doctor

Inactive Ingrediens

Water, Butyloctyl Salicylate , Propanediol, Glycerin, C12-C15 Alkyl Benzoate, Blyceryl Stearate Citrate, Isododecane, Niacinamide, Polymethylsilsesquioxane, Mica, Glyceryl Stearate, Titanium Dioxide, Iron Oxides, Caprylic/Capric Triglyceride, Cetyl Phosphate, Diisopropyl Sabacate, Isododecyl Neopentanoate, Lauryl Lactate, Coco-Caprylate, Bismuth Oxychloride, Arginine, Butylene Glycol, 1,2-Hexanediol, Caprylyl Glycol, Hydroxyacetophenone, Ethylhexyl Hudroxystearate, Sodium Hyaluronate, Chlorphenesin, Acrylates/C10-C30 Alkyl Acrylate Crosspolymer, Trisodium Ethylenediamine Disuccinate, Phospholipds, Limonium Gerberi Extract, Leuconostoc/Radish Root Ferment Filtrate, Theobroma Cacao (Cocoa) Seed Extract, Pantothenic Acid, Triethoxycprylylsilane, Tocopherol, Ferulic Acid, Helianthus Annus (Sunflower) Seed Oil

Package Label/PDP

Supergoop! Glow Screen SPF 40 GoldenHour Broad Spectrum Sunscren SPF 40 PA +++ 1.7 fl. oz. / 50 mL

Supergoop! Glowscreen Golden Hour 20 ml

Supergoop! Glowscreen Golden Hour 10 ml

INGREDIENTS AND APPEARANCE

SUPERGOOP GLOW SCREEN SPF 40  SHADE 2 GOLDEN HOUR
broad spectrum sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75936-601
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	4 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
PANTOTHENIC ACID (UNII: 19F5HK2737)
FERULIC ACID (UNII: AVM951ZWST)
ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
TOCOPHEROL (UNII: R0ZB2556P8)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85)
COCO-CAPRYLATE (UNII: 4828G836N6)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
CHLORPHENESIN (UNII: I670DAL4SZ)
THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CETYL PHOSPHATE (UNII: VT07D6X67O)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
LAURYL LACTATE (UNII: G5SU0BFK7O)
ARGININE (UNII: 94ZLA3W45F)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
GLYCERIN (UNII: PDC6A3C0OX)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
NIACINAMIDE (UNII: 25X51I8RD4)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
ISODODECANE (UNII: A8289P68Y2)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
WATER (UNII: 059QF0KO0R)
C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
LIMONIUM GERBERI WHOLE (UNII: 2J5K7YCF9F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75936-601-02	1 in 1 BOX	12/20/2021
1	NDC: 75936-601-01	50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 75936-601-03	10 mL in 1 TUBE; Type 0: Not a Combination Product	12/20/2021
3	NDC: 75936-601-04	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	12/20/2021
4	NDC: 75936-601-06	1 in 1 BOX	12/20/2021
4	NDC: 75936-601-05	20 mL 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	12/20/2021

Labeler - Supergoop LLC (117061743)