FDA.reportPublic FDA data

Sonni SunDay Body Balm

Manufacturer
Sonni
Effective date
2025-10-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:40:04

Label at a glance#

ProductSonni SunDay Body Balm
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sonni SunDay Body Balm

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sonni SunDay Body Balm

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Sonni SunDay Body Balm

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Sonni SunDay Body Balm

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Sonni SunDay Body Balm

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Sonni SunDay Body Balm

OTC - PURPOSE SECTION

PurposePurpose

Sonni SunDay Body Balm

WARNINGS SECTION

WarningWarning

Sonni SunDay Body Balm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85260-492-01Sonni SunDay Body Balm150000 mL in 1 BOTTLE, PUMPLOTION1500001
85260-492-02Sonni SunDay Body Balm1 in 1 CARTONLOTION11

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85260-49285260-492-01, 85260-492-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARETH-20L0Q8IK9E08IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ALLANTOIN344S277G0ZIACT
CETYL ALCOHOL936JST6JCNIACT
PULLULAN8ZQ0AYU1TTIACT
CAPRYLYL GLYCOL00YIU5438UIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
AVENA SATIVA WHOLE5P8D0Z74RGIACT
POLYESTER-70841698D2FIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
TRICETEARETH-4 PHOSPHATE69534Y66NOIACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
C12-20 ALKYL BENZOATEY15I6XI14CIACT
ZINC OXIDESOI2LOH54ZACTIB
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ETHYLHEXYL ISONONANOATEI6KB4GE3K4IACT
SQUALANEGW89575KF9IACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT

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 Body BalmTITANIUM DIOXIDE, ZINC OXIDESonni41adca2e-cf69-ccd9-e063-6294a90a0dc02025-10-21WarningsExact identifier
ndc (package): 85260-492-02
ndc (package): 85260-492-01
ndc (product): 85260-492
ndc11 (package): 85260049202
ndc11 (package): 85260049201
spl id: 41adca2e-cf6b-ccd9-e063-6294a90a0dc0
spl set id: 41adca2e-cf69-ccd9-e063-6294a90a0dc0

Reported adverse events (FAERS/openFDA)#

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