FDA.reportPublic FDA data

Wonderscreen Broad Spectrum SPF 30

Manufacturer
Dime Beauty Co, LLC
Effective date
2025-10-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:15:30

Label at a glance#

ProductWonderscreen Broad Spectrum SPF 30
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Zinc Oxide

Purpose: Sunscreen

OTC - PURPOSE SECTION

Uses: Helps prevent sunburn. Higher SPF gives more sunburn protection

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.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs.

WARNINGS SECTION

Warning:

  • For External use only. Do not use on broken or damaged skin

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Apply liberally 15 minutes before sun or water exposure
  • Immediately after towel drying
  • At least every 2 hours
  • Children under 6 months: ask a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Ethylhexyl Olivate, Dimethicone, C9-12 Alkane, Cocoglycerides, Hydroxyethyl Dimethicone Laurate, Pentylene Glycol, Butyloctyl Salicylate, Glycerin, Jojoba Esters, Pyrus Malus (Apple) Fruit Extract, Polymethylsilsesquioxane, Squalane, Dipotassium Glycyrrhizate, Beta Vulgaris (Beet) Root Extract, Fructooligosaccharides, Glycine Soja (Soybean) Seed Extract Diheptyl Succinate, Disteardimonium Hectorite, Phenoxyethanol, Sodium Chloride, Polyhydroxystearic Acid, Trihydroxystearin, Triethyl Citrate, Hydroxyacetophenone, Sodium Citrate, Tetrasodium Glutamate Diacetate, Sodium Dehydroacetate, Capryloyl Glycerin/Sebacic Acid Copolymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DIME

Wonderscreen

Broad Spectrum SPF 30

50 G

Wonderscreen SPF 30 BoxWonderscreen SPF 30 Box

Pump bottlePump bottle

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82870-001-01Wonderscreen Broad Spectrum SPF 3050 g in 1 BOTTLE, PUMPCREAM504

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
82870-00182870-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIHYDROXYSTEARIN06YD7896S3IACT
PENTYLENE GLYCOL50C1307PZGIACT
DIMETHICONE 100RO266O364UIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
SODIUM CITRATE1Q73Q2JULRIACT
SODIUM CHLORIDE451W47IQ8XIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
SQUALANEGW89575KF9IACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
BEETN487KM8COKIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
GLYCERINPDC6A3C0OXIACT
COCO-GLYCERIDESISE9I7DNUGIACT
APPLEB423VGH5S9IACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
PHENOXYETHANOLHIE492ZZ3TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
SODIUM DEHYDROACETATE8W46YN971GIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT

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
Wonderscreen Broad Spectrum SPF 30ZINC OXIDEDime Beauty Co, LLCe38deed3-e1e2-0b1d-e053-2a95a90a547f2025-10-01WarningsExact identifier
ndc (package): 82870-001-01
ndc (product): 82870-001
ndc11 (package): 82870000101
spl id: 401d6a89-6194-f287-e063-6294a90aca43
spl set id: e38deed3-e1e2-0b1d-e053-2a95a90a547f

Reported adverse events (FAERS/openFDA)#

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