FDA.reportPublic FDA data

Hanalei Face Moisturizing

Manufacturer
Hanalei Beauty Company LLC
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:15:59

Label at a glance#

ProductHanalei Face Moisturizing
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Hanalei Face Moisturizing

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Hanalei Face Moisturizing

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Hanalei Face Moisturizing

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Hanalei Face Moisturizing

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Hanalei Face Moisturizing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Hanalei Face Moisturizing

OTC - PURPOSE SECTION

purposepurpose

Hanalei Face Moisturizing

WARNINGS SECTION

Warning LabelWarning Label

Hanalei Face Moisturizing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82915-2133-1Hanalei Face Moisturizing50 mL in 1 TUBELOTION503
82915-2133-2Hanalei Face Moisturizing1 in 1 CARTONLOTION13

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
82915-213382915-2133-1, 82915-2133-2

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
LAVANDULA ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
ALLANTOIN344S277G0ZIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
XANTHAN GUMTTV12P4NEEIACT
ISOAMYL LAURATEM1SLX00M3MIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
TOCOPHEROLR0ZB2556P8IACT
CETYL ALCOHOL936JST6JCNIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
WATER059QF0KO0RIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CETETH-20I835H2IHHXIACT
PULLULAN8ZQ0AYU1TTIACT
SQUALANEGW89575KF9IACT
STEARETH-20L0Q8IK9E08IACT
ZINC OXIDESOI2LOH54ZACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
PEG-75 STEARATEOT38R0N74HIACT

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
Hanalei Face MoisturizingZINC OXIDEHanalei Beauty Company LLC1f7c1a68-5aea-0deb-e063-6394a90a3a432025-11-13WarningsExact identifier
ndc (package): 82915-2133-2
ndc (package): 82915-2133-1
ndc (product): 82915-2133
ndc11 (package): 82915213302
ndc11 (package): 82915213301
spl id: 437faecc-14d2-a2de-e063-6394a90a429a
spl set id: 1f7c1a68-5aea-0deb-e063-6394a90a3a43

Reported adverse events (FAERS/openFDA)#

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