FDA.reportPublic FDA data

Sonni SunDay Serum

Manufacturer
Sonni
Effective date
2025-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:39:36

Label at a glance#

ProductSonni SunDay Serum
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sonni SunDay Serum

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sonni SunDay Serum

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Sonni SunDay Serum

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Sonni SunDay Serum

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Sonni SunDay Serum

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Sonni SunDay Serum

OTC - PURPOSE SECTION

PurposePurpose

Sonni SunDay Serum

WARNINGS SECTION

WarningWarning

Sonni SunDay Serum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85260-282-01Sonni SunDay Serum50 mL in 1 BOTTLE, DROPPERLOTION501
85260-282-02Sonni SunDay Serum1 in 1 CARTONLOTION11

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85260-28285260-282-01, 85260-282-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
PALMITOYL TETRAPEPTIDE-7Q41S464P1RIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ISODODECANEA8289P68Y2IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ZINC OXIDESOI2LOH54ZACTIB
POLYSORBATE 207T1F30V5YHIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
GLYCERINPDC6A3C0OXIACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
CARRAGEENAN5C69YCD2YJIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PALMITOYL TRIPEPTIDE-1RV743D216MIACT
.BETA.-TOCOPHEROL9U6A490501IACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT

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
Sonni SunDay SerumZINC OXIDESonni419d4ada-fe9b-b774-e063-6394a90a3d092025-10-20WarningsExact identifier
ndc (package): 85260-282-01
ndc (package): 85260-282-02
ndc (product): 85260-282
ndc11 (package): 85260028202
ndc11 (package): 85260028201
spl id: 419d3622-3cf2-b28f-e063-6394a90a5ba5
spl set id: 419d4ada-fe9b-b774-e063-6394a90a3d09

Reported adverse events (FAERS/openFDA)#

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