FDA.reportPublic FDA data

Latin Beauty LLC. Powder Sunscreen SPF 50 Kiss the Sun

Manufacturer
Guangzhou Yueyou Biological Technology Co., Ltd.
Effective date
2025-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:00

Label at a glance#

ProductLatin Beauty LLC. Powder Sunscreen SPF 50 Kiss the Sun
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosagedosage

WARNINGS SECTION

warningwarning

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INDICATIONS & USAGE SECTION

usageusage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out reach of childrenkeep out reach of children

OTC - PURPOSE SECTION

purposepurpose

Latin Beauty LLC. Powder Sunscreen SPF 50 Kiss the Sun

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Latin Beauty LLC. Powder Sunscreen SPF 50 Kiss the Sun

sunscreen powdersunscreen powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85473-443-06Latin Beauty LLC. Powder Sunscreen SPF 50 Kiss the Sun6 g in 1 BOTTLEPOWDER61

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85473-44385473-443-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
NYLON-12446U8J075BIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CI 77492EX438O2MRTIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
SILICA, TRIMETHYLSILYL CAPPEDVU10KU4B9SIACT
CI 774911K09F3G675IACT
MICAV8A1AW0880IACT
NIACINAMIDE25X51I8RD4IACT
ALOE BARBADENSIS LEAF POWDERZY81Z83H0XIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIPOTASSIUM GLYCYRRHIZATECA2Y0FE3FXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ZINC OXIDESOI2LOH54ZACTIB
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT

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
3b31c5c1-0faf-d622-e063-6394a90a39313b31c5c1-0fae-d622-e063-6394a90a39312025-07-30WarningsExact identifier
spl id: 3b31c5c1-0faf-d622-e063-6394a90a3931
spl set id: 3b31c5c1-0fae-d622-e063-6394a90a3931

Reported adverse events (FAERS/openFDA)#

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