FDA.reportPublic FDA data

Naturium Dew Glow Moisturizer Mineral SPF 50

Manufacturer
e.l.f. Cosmetics, Inc
Effective date
2026-02-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-06 05:10:19

Label at a glance#

ProductNaturium Dew Glow Moisturizer Mineral SPF 50
Active ingredientZINC OXIDE
Label structure8 sections

Dosage and administration

Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours. Use water resistant sunscreen if swimming or sweating. 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 sun, especially from 10 a.m.-2 p.m., wear lo...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 10%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE 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.

Warning

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product:

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours.
  • Use water resistant sunscreen if swimming or sweating.
  • 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 sun, especially from 10 a.m.-2 p.m., wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: ask a doctor.

Other Information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Glycerin, C13-15 Alkane, Butyloctyl Salicylate, Tridecyl Salicylate, Diethylhexyl 2,6-Naphthalate, Calcium Sodium Borosilicate, Ethylhexyl Methoxycrylene, Mica, Propanediol, Galactoarabinan, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyricinoleic Acid, Niacinamide, Dimethicone, Sodium Cocoyl Glutamate, Phenoxyethanol, C15-23 Alkane, Polyglyceryl-3 Polyricinoleate, Sorbitan Isostearate, Hydrogenated Castor Oil/Sebacic Acid Copolymer, Hydroxyacetophenone, Lauryl Laurate, Oryzanol, Coconut Oil Ethyl Ferulate Esters, C13-14 Alkane, Decyl Glucoside, Bisabolol, Squalane, Sodium Phytate, 3-O-Ethyl Ascorbic Acid, Hippophae Rhamnoides Fruit Oil, Tocopheryl Acetate, Sodium Hyaluronate.

Questions or comments?

OTC - QUESTIONS SECTION

1-888-315-9814

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label_Dew Glow MineralPackage Label_Dew Glow Mineral

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76354-30076354-300-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 matching rows.

Name, UNII, Kind table
NameUNIIKind
3-O-ETHYL ASCORBIC ACID6MW60CB71PIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM HYALURONATEYSE9PPT4THIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
C13-15 ALKANE114P5I43UJIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
CALCIUM SODIUM BOROSILICATE4MM76N4WMYIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
MICAV8A1AW0880IACT
PROPANEDIOL5965N8W85TIACT
GALACTOARABINANSL4SX1O487IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
POLYGLYCEROL POLYRICINOLEIC ACID3C96Y1D5T4IACT
NIACINAMIDE25X51I8RD4IACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM COCOYL GLUTAMATEBMT4RCZ3HGIACT
PHENOXYETHANOLHIE492ZZ3TIACT
C15-23 ALKANEJ3N6X3YK96IACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
HYDROGENATED CASTOR OIL/SEBACIC ACID COPOLYMERH7DBQ4WF5MIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
LAURYL LAURATEGPW77G0937IACT
ORYZANOLSST9XCL51MIACT
COCONUT OILQ9L0O73W7LIACT
ETHYL FERULATE5B8915UELWIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
DECYL GLUCOSIDEZ17H97EA6YIACT
BISABOLOL24WE03BX2TIACT
SQUALANEGW89575KF9IACT
SODIUM PHYTATE88496G1ERLIACT
ZINC OXIDESOI2LOH54ZACTIB
HIPPOPHAE RHAMNOIDES FRUIT OILTA4JCF9S1JIACT

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
Naturium Dew Glow Moisturizer Mineral SPF 50ZINC OXIDEe.l.f. Cosmetics, Inc535f798f-d21d-92b2-e063-6294a90a72c72026-02-02WarningsExact identifier
ndc (package): 76354-300-01
ndc (product): 76354-300
ndc11 (package): 76354030001
spl id: 535f64d1-5ef3-92b4-e063-6294a90a0f0c
spl set id: 535f798f-d21d-92b2-e063-6294a90a72c7

Reported adverse events (FAERS/openFDA)#

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