EVERY. SINGLE. FACE. WATERY SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion

Every. Single. Face. Watery SPF 50 by

Drug Labeling and Warnings

Every. Single. Face. Watery SPF 50 by is a Otc medication manufactured, distributed, or labeled by Supergoop, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Avobenzone 3% Sunscreen

Homosalate 9%

Octisalate 5%

Octocrylene 9%

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 & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

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 & ADMINISTRATION

Directions

• apply generously and evenly 15 minutes before sun exposure

reapply:

• after 40 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 early skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF calue of 15 or higher and other sun protection measures including:

• Limit time in the sun, especially from 10 a.m.-2p.m.
• Wear long-sleeved shirts, pants, hats, and sunglasses
• Reapply at least every 2 hours
• Children under 6 months: Ask a doctor

INACTIVE INGREDIENT

Inactive Ingredients: Water, Alcohol Denat., C12-15 Alkyl Benzoate, Propanediol, Dimethicone, Glycerin,
Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Maltodextrin, Hydroxyacetophenone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, 1,2 Hexanediol, Caprylyl Glycol, Pullulan, Sodium Polyacrylate, Betaine, Hedychium Coronarium Root Extract, Caesalpinia Spinosa Gum, Tremella Fuciformis Sporocarp Extract, Glyceryl Caprylate, Glyceryl Undecylenate, Sodium Carboxymethyl Beta-Glucan, Lepidium Sativum Sprout Extract.

OTHER SAFETY INFORMATION

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

PRINCIPAL DISPLAY PANEL

Supergoop!

EVERY. SINGLE. FACE.

WATERY LOTION

SPF 50

Broad Spectrum Sunscreen SPF 50 PA++++

Water & Sweat Resistant (40 minutes)

1.7 fl. oz./ 50 ml.

INGREDIENTS AND APPEARANCE

EVERY. SINGLE. FACE. WATERY SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75936-652
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
PROPANEDIOL (UNII: 5965N8W85T)
DIMETHICONE (UNII: 92RU3N3Y1O)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PULLULAN (UNII: 8ZQ0AYU1TT)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)
HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
BETAINE (UNII: 3SCV180C9W)
GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75936-652-01	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	01/15/2022
2	NDC: 75936-652-02	10 mL in 1 TUBE; Type 0: Not a Combination Product	01/15/2022
3	NDC: 75936-652-03	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/11/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/11/2021

Labeler - Supergoop, LLC (117061743)