DEWSCREEN DAILY HYDRATOR AND PRIMER SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion

Dewscreen Daily Hydrator and Primer SPF 50 by

Drug Labeling and Warnings

Dewscreen Daily Hydrator and Primer 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:

Avobenzone 3.0%
Homosalate 9.0%
Octisalate 4.5%
Octocrylene 9.0%

PURPOSE

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

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

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

Directions

Apply generously and evenly as the last step in your skincare routine, before makeup and 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Children under 6 months of age: ask a doctor. 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 sunglasses.

INACTIVE INGREDIENT

Inactive Ingredients:

Water, Acrylates/Steareth-20 Methacrylate Copolymer, Pentylene Glycol, Glycerin, Isododecane, Palmitoyl Tripeptide-5, Tremella Fuciformis Sporocarp Extract, Hydrolyzed Hyaluronic Acid, Carthamus Tinctorius (Safflower) Oleosomes, Bisabolol, Dimethicone Crosspolymer-3, Trisodium Ethylenediamine Disuccinate, Betaine, Polyglutamic Acid, Sodium Benzoate, Sodium Hydroxide, Potassium Sorbate

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs

PRINCIPAL DISPLAY PANEL

Supergoop!

DEW

SCREEN

Daily Hydrator

+ Primer

SPF 50

Polyglutamic Peptide Complex

Broad Spectrum Sunscreen

SPF 50 PA++++

1.7 fl. oz. / 50 mL or 0.34 fl. oz / 10 mL

INGREDIENTS AND APPEARANCE

DEWSCREEN DAILY HYDRATOR AND PRIMER SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75936-660
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
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
BISABOLOL (UNII: 24WE03BX2T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYGLUTAMIC ACID (1200 MW) (UNII: MGE3733FR2)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
DIMETHICONE CROSSPOLYMER (UNII: UF7620L1W6)
PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
ACRYLATES/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
HYALURONIC ACID (UNII: S270N0TRQY)
BETAINE (UNII: 3SCV180C9W)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
GLYCERIN (UNII: PDC6A3C0OX)
ISODODECANE (UNII: A8289P68Y2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75936-660-02	1 in 1 CARTON	11/01/2025
1	NDC: 75936-660-01	50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 75936-660-03	10 mL in 1 TUBE; Type 0: Not a Combination Product	11/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/01/2025

Labeler - Supergoop LLC (117061743)