FDA.reportPublic FDA data

Luminess SPF30 Suncreen Setting Powder

Manufacturer
Kinetics Derma Beauty, L.L.C
Effective date
2024-06-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:00:47

Label at a glance#

ProductLuminess SPF30 Suncreen Setting Powder
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Luminess SPF 30 Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Luminess SPF 30 dosage and administration

DOSAGE & ADMINISTRATION SECTION

Dosage and administrationDosage and administration

Luminess SPF 30 Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Luminess SPF 30 Purpose

OTC - PURPOSE SECTION

PurposePurpose

Luminess SPF 30 Usage

INDICATIONS & USAGE SECTION

UsageUsage

Luminess SPF 30 warnings

WARNINGS SECTION

WArningsWArnings

Luminess SPF Instructions for use

INSTRUCTIONS FOR USE SECTION

InstructionsInstructions

Luminess SPF 30 Principle display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

principle Display panelprinciple Display panel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73368-150LUMINESS SPF30 SUNCREEN SETTING POWDER (ZINC OXIDE,TITANIUM DIOXIDE) POWDER [KINETICS DERMA BEAUTY, L.L.C]3Legacy NDC20240614_a83aefe2-d1e1-432c-e053-2995a90a7d28.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73368-15073368-150-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
POTASSIUM HYDROLYZED JOJOBA ESTERSCH428W5O62IACT
BISMUTH OXYCHLORIDE4ZR792I587IACT
CHLORPHENESINI670DAL4SZIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
MAGNESIUM MYRISTATEZ1917F0578IACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
THEOBROMA GRANDIFLORUM SEED BUTTERI711F13FXMIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
BORON NITRIDE2U4T60A6YDIACT
ISOPROPYL ALCOHOLND2M416302IACT

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
1ab79168-59b2-0721-e063-6294a90ac7e3a83aefe2-d1e1-432c-e053-2995a90a7d282024-06-12WarningsExact identifier
spl id: 1ab79168-59b2-0721-e063-6294a90ac7e3
spl set id: a83aefe2-d1e1-432c-e053-2995a90a7d28

Reported adverse events (FAERS/openFDA)#

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