FDA.reportPublic FDA data

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

Manufacturer
Eco-Chic LLC
Effective date
2025-10-16
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:39:24

Label at a glance#

ProductELEVEN BY VENUS WILLIAMS ACE THE DAY Face
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

OTC - PURPOSE SECTION

purposepurpose

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

WARNINGS SECTION

Warning LabelWarning Label

ELEVEN BY VENUS WILLIAMS ACE THE DAY Face

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850015162640GTIN-13: 0850015162640
EAN-13: 0850015162640
GTIN-12: 850015162640
UPC-A: 850015162640
GTIN storage (14 digits): 00850015162640		Eleven Face Lotion SPF 30 Secondary_OL (3).jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79163-386-01ELEVEN BY VENUS WILLIAMS ACE THE DAY Face50 mL in 1 BOTTLELOTION505
79163-386-02ELEVEN BY VENUS WILLIAMS ACE THE DAY Face1 in 1 CARTONLOTION15

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
79163-38679163-386-01, 79163-386-02

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
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
RUTIN5G06TVY3R7IACT
GLYCERINPDC6A3C0OXIACT
ISOAMYL LAURATEM1SLX00M3MIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TOCOPHEROLR0ZB2556P8IACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
METHYLPROPANEDIOLN8F53B3R4RIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
ALLANTOIN344S277G0ZIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
C13-15 ALKANE114P5I43UJIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-08-14full-release2026-06-01 01:10:45

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
ELEVEN BY VENUS WILLIAMS ACE THE DAY FaceZINC OXIDEEco-Chic LLCde438665-72d9-9b1b-e053-2a95a90ab9ef2025-10-16WarningsExact identifier
ndc (package): 79163-386-01
ndc (package): 79163-386-02
ndc (product): 79163-386
ndc11 (package): 79163038602
ndc11 (package): 79163038601
spl id: 414901b3-bac9-9e20-e063-6294a90a9f50
spl set id: de438665-72d9-9b1b-e053-2a95a90ab9ef

Reported adverse events (FAERS/openFDA)#

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