Dewscreen Daily Hydrator and Primer SPF 50

Manufacturer
Supergoop LLC
Effective date
2025-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:41:14

Label at a glance#

ProductDewscreen Daily Hydrator and Primer SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

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

OTC - PURPOSE SECTION

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 SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help, or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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 SECTION

Stop use and ask a doctor if rash occurs

PACKAGE LABEL.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

50 mL Primary50 mL Primary50 mL Secondary50 mL Secondary10 mL Primary10 mL Primary

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-660-01Dewscreen Daily Hydrator and Primer SPF 5050 mL in 1 TUBELOTION501
75936-660-02Dewscreen Daily Hydrator and Primer SPF 501 in 1 CARTONLOTION11
75936-660-03Dewscreen Daily Hydrator and Primer SPF 5010 mL in 1 TUBELOTION101

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-66075936-660-01, 75936-660-02, 75936-660-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dewscreen Daily Hydrator and Primer SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENESupergoop LLC3f7c84e3-0e4f-b7e9-e063-6294a90a12952025-09-23WarningsExact identifier
ndc (package): 75936-660-03
ndc (package): 75936-660-02
ndc (package): 75936-660-01
ndc (product): 75936-660
ndc11 (package): 75936066002
ndc11 (package): 75936066001
ndc11 (package): 75936066003
spl id: 3f7c84e3-0e50-b7e9-e063-6294a90a1295
spl set id: 3f7c84e3-0e4f-b7e9-e063-6294a90a1295

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.