FDA.reportPublic FDA data

Alleyoop Sunsational Broad Spectrum

Manufacturer
NewAlley Innovations Inc
Effective date
2025-09-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:14:39

Label at a glance#

ProductAlleyoop Sunsational Broad Spectrum
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Alleyoop Sunsational Broad Spectrum

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Alleyoop Sunsational Broad Spectrum

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Alleyoop Sunsational Broad Spectrum

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Alleyoop Sunsational Broad Spectrum

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Alleyoop Sunsational Broad Spectrum

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Alleyoop Sunsational Broad Spectrum

OTC - PURPOSE SECTION

PurposePurpose

Alleyoop Sunsational Broad SpectrumAlleyoop Sunsational Broad Spectrum

WARNINGS SECTION

WarningWarning

Alleyoop Sunsational Broad Spectrum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84830-2431-1Alleyoop Sunsational Broad Spectrum30 mL in 1 TUBELOTION303
84830-2431-2Alleyoop Sunsational Broad Spectrum1 in 1 CARTONLOTION13
84830-2431-3Alleyoop Sunsational Broad Spectrum30 mL in 1 BOTTLELOTION303
84830-2431-4Alleyoop Sunsational Broad Spectrum1 in 1 CARTONLOTION13

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84830-243184830-2431-1, 84830-2431-2, 84830-2431-3, 84830-2431-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4IACT
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
SODIUM CHLORIDE451W47IQ8XIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
CAPRYLYL GLYCOL00YIU5438UIACT
SODIUM HYDROXIDE55X04QC32IIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
ROSMARINUS OFFICINALIS WHOLEEA3289138MIACT
METHYLHEPTYL ISOSTEARATE981F40Q9FFIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
COCO-CAPRYLATE4828G836N6IACT
TOCOPHEROLR0ZB2556P8IACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
MICAV8A1AW0880IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
ALLANTOIN344S277G0ZIACT
FERRIC OXIDE RED1K09F3G675IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
CALCIUM SODIUM BOROSILICATE4MM76N4WMYIACT
DIMETHICONE 100RO266O364UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ZINC OXIDESOI2LOH54ZACTIB
HELIANTHUS ANNUUS WHOLE17S27ZT6KRIACT

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
Alleyoop Sunsational Broad SpectrumZINC OXIDENewAlley Innovations Inc248419c4-8044-402c-e063-6394a90a00f82025-09-24WarningsExact identifier
ndc (package): 84830-2431-2
ndc (package): 84830-2431-4
ndc (package): 84830-2431-1
ndc (package): 84830-2431-3
ndc (product): 84830-2431
ndc11 (package): 84830243103
ndc11 (package): 84830243101
ndc11 (package): 84830243104
ndc11 (package): 84830243102
spl id: 3f927b1c-ba51-3ed0-e063-6294a90a8f8a
spl set id: 248419c4-8044-402c-e063-6394a90a00f8

Reported adverse events (FAERS/openFDA)#

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