FDA.reportPublic FDA data

Golden Rays Sunscreen (Light Tinted)

Manufacturer
A-Frame SunCo Inc | Nanophase Technologies Corporation
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:52:21

Label at a glance#

ProductGolden Rays Sunscreen (Light Tinted)
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Golden Rays Sunscreen (Light Tinted)

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Golden Rays Sunscreen (Light Tinted)

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Golden Rays Sunscreen (Light Tinted)

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Golden Rays Sunscreen (Light Tinted)

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Golden Rays Sunscreen (Light Tinted)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Golden Rays Sunscreen (Light Tinted)

OTC - PURPOSE SECTION

purposepurpose

Golden Rays Sunscreen (Light Tinted)

WARNINGS SECTION

Warning LabelWarning Label

Golden Rays Sunscreen (Light Tinted)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82184-1351-1Golden Rays Sunscreen (Light Tinted)28 mL in 1 BOTTLE, PUMPLOTION284
82184-1351-2Golden Rays Sunscreen (Light Tinted)1 in 1 CARTONLOTION14
82184-1351-3Golden Rays Sunscreen (Light Tinted)60 mL in 1 BOTTLELOTION604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82184-1351GOLDEN RAYS SUNSCREEN (LIGHT TINTED) (ZINC OXIDE) LOTION [A-FRAME SUNCO INC]4Legacy NDC, 3 package rows20250112_d9b612b6-af34-d3d1-e053-2995a90af83f.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82184-135182184-1351-1, 82184-1351-2, 82184-1351-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
GLYCERINPDC6A3C0OXIACT
TOCOPHEROLR0ZB2556P8IACT
FERRIC OXIDE RED1K09F3G675IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
ALLANTOIN344S277G0ZIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
DIMETHICONE92RU3N3Y1OIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ISODODECANEA8289P68Y2IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ZINC OXIDESOI2LOH54ZACTIB
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT

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
2b47aef4-ba48-52df-e063-6394a90ab2a7d9b612b6-af34-d3d1-e053-2995a90af83f2025-01-09WarningsExact identifier
spl id: 2b47aef4-ba48-52df-e063-6394a90ab2a7
spl set id: d9b612b6-af34-d3d1-e053-2995a90af83f

Reported adverse events (FAERS/openFDA)#

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