FDA.reportPublic FDA data

Svens Everyday Mineral Sunscreen

Manufacturer
Svens, Inc
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:16:10

Label at a glance#

ProductSvens Everyday Mineral Sunscreen
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Svens Everyday Mineral Sunscreen

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Svens Everyday Mineral Sunscreen

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Svens Everyday Mineral Sunscreen

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Svens Everyday Mineral Sunscreen

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Svens Everyday Mineral Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Svens Everyday Mineral Sunscreen

OTC - PURPOSE SECTION

purposepurpose

Svens Everyday Mineral Sunscreen

WARNINGS SECTION

Warning LabelWarning Label

Svens Everyday Mineral Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Svens Sunscreen labelSvens Sunscreen label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860000810708GTIN-13: 0860000810708
EAN-13: 0860000810708
GTIN-12: 860000810708
UPC-A: 860000810708
GTIN storage (14 digits): 00860000810708		Svens Sunscreen label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72743-4314-12024-10-06C16284748780-1f386c649-c411-0266-e053-dadaa90a7c1aSvens Everyday Mineral Sunscreen
72743-4314-12023-01-30C16284748780-1f386c649-c411-0266-e053-dadaa90a7c1aSvens Everyday Mineral Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72743-4314-1Svens Everyday Mineral Sunscreen100 mL in 1 TUBELOTION1004

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72743-431472743-4314-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLYL GLYCOL00YIU5438UIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PULLULAN8ZQ0AYU1TTIACT
STEARETH-20L0Q8IK9E08IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ALLANTOIN344S277G0ZIACT
CETYL ALCOHOL936JST6JCNIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
AVENA SATIVA WHOLE5P8D0Z74RGIACT
POLYESTER-70841698D2FIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
TRICETEARETH-4 PHOSPHATE69534Y66NOIACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
C12-20 ALKYL BENZOATEY15I6XI14CIACT
ZINC OXIDESOI2LOH54ZACTIB
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ETHYLHEXYL ISONONANOATEI6KB4GE3K4IACT
SQUALANEGW89575KF9IACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT

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
Svens Everyday Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDESvens, Inc912170ae-124c-5eb9-e053-2995a90a0ba32025-11-14WarningsExact identifier
ndc (package): 72743-4314-1
ndc (product): 72743-4314
ndc11 (package): 72743431401
spl id: 4390c914-f2cc-9681-e063-6394a90ac9d9
spl set id: 912170ae-124c-5eb9-e053-2995a90a0ba3

Reported adverse events (FAERS/openFDA)#

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