FDA.reportPublic FDA data

Knesko Skin The Sunscreen

Manufacturer
Knesko, LLC
Effective date
2026-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:16

Label at a glance#

ProductKnesko Skin The Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Knesko Skin The Sunscreen

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Knesko Skin The Sunscreen

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Knesko Skin The Sunscreen

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Knesko Skin The Sunscreen

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Knesko Skin The Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Knesko Skin The Sunscreen

OTC - PURPOSE SECTION

PurposePurpose

Knesko Skin The Sunscreen

WARNINGS SECTION

WarningWarning

Knesko Skin The Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeknesko.me/the_sunscreenKnesko The Sunscreen.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87407-236-01Knesko Skin The Sunscreen50 mL in 1 BOTTLELOTION501
87407-236-02Knesko Skin The Sunscreen1 in 1 CARTONLOTION11

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87407-23687407-236-01, 87407-236-02

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
SILICON DIOXIDEETJ7Z6XBU4IACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
LECITHIN, SOYBEAN1DI56QDM62IACT
DIMETHICONE 200RGS4T2AS00IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ISODODECANEA8289P68Y2IACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALLANTOIN344S277G0ZIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
C13-15 ALKANE114P5I43UJIACT
SODIUM HYDROXIDE55X04QC32IIACT
CALCIUM SODIUM BOROSILICATE4MM76N4WMYIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CAPRYLYL GLYCOL00YIU5438UIACT

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
Knesko Skin The SunscreenZINC OXIDEKnesko, LLC5114dc75-a865-326e-e063-6294a90a89112026-05-05WarningsExact identifier
ndc (package): 87407-236-02
ndc (package): 87407-236-01
ndc (product): 87407-236
ndc11 (package): 87407023601
ndc11 (package): 87407023602
spl id: 5114ef81-229c-690c-e063-6394a90a0cd0
spl set id: 5114dc75-a865-326e-e063-6294a90a8911

Reported adverse events (FAERS/openFDA)#

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