FDA.reportPublic FDA data

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

Manufacturer
Ilia, Inc.
Effective date
2026-05-21
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:58:33

Label at a glance#

ProductILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

OTC - PURPOSE SECTION

purposepurpose

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

WARNINGS SECTION

Warning LabelWarning Label

ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130818107027024GTIN-13: 0818107027024
EAN-13: 0818107027024
GTIN-12: 818107027024
UPC-A: 818107027024
GTIN storage (14 digits): 00818107027024		ILIA Shade 9.5 Unit Carton Label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81110-052-01ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)30 mL in 1 BOTTLE, DROPPERLOTION307
81110-052-02ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)1 in 1 CARTONLOTION17

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81110-05281110-052-01, 81110-052-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
FERRIC OXIDE RED1K09F3G675IACT
HYALURONATE SODIUMYSE9PPT4THIACT
SHEA BUTTERK49155WL9YIACT
ISOAMYL LAURATEM1SLX00M3MIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
ISOPROPYL ISOSTEARATEC67IXB9Y7TIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
CAPRYLYL GLYCOL00YIU5438UIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
ALOE VERA LEAFZY81Z83H0XIACT
ALLANTOIN344S277G0ZIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SQUALANEGW89575KF9IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM MYRISTOYL GLUTAMATEAYU7QD893WIACT
ZINC OXIDESOI2LOH54ZACTIB
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
PROPANEDIOL5965N8W85TIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENYLPROPANOL0F897O3O4MIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62025-10-30monthly-update2026-06-03 17:39:08
52025-08-14full-release2026-06-01 01:10:43

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
ILIA SUPER SERUM SKIN TINT (ST9.5 BAIKAL)ZINC OXIDEIlia, Inc.b97f7fe9-c06e-7c11-e053-2a95a90a6a6d2026-05-21WarningsExact identifier
ndc (package): 81110-052-02
ndc (package): 81110-052-01
ndc (product): 81110-052
ndc11 (package): 81110005201
ndc11 (package): 81110005202
spl id: 52599eae-59e6-4a61-e063-6294a90adc39
spl set id: b97f7fe9-c06e-7c11-e053-2a95a90a6a6d

Reported adverse events (FAERS/openFDA)#

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