FDA.reportPublic FDA data

dAlba Vegan Fresh Sun Stick

Manufacturer
ADMTMAX LLC | Kolmar Korea Co., Ltd
Effective date
2025-06-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:02:37

Label at a glance#

ProductdAlba Vegan Fresh Sun Stick
Active ingredientHOMOSALATE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosagedosage

WARNINGS SECTION

warning 4warning 4

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INDICATIONS & USAGE SECTION

indicationindication

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

children out reachchildren out reach

OTC - PURPOSE SECTION

purposepurpose

OTC - ACTIVE INGREDIENT SECTION

activeactive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Main DisplayMain Display

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84662-050-04dAlba Vegan Fresh Sun Stick19 g in 1 CARTRIDGECREAM192

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84662-05084662-050-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT

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
dAlba Vegan Fresh Sun StickHOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATEADMTMAX LLC20ae82ae-bc8f-89d1-e063-6394a90afff22025-06-08WarningsExact identifier
ndc (package): 84662-050-04
ndc (product): 84662-050
ndc11 (package): 84662005004
spl id: 371bf6ac-7459-8e82-e063-6394a90acc77
spl set id: 20ae82ae-bc8f-89d1-e063-6394a90afff2

Reported adverse events (FAERS/openFDA)#

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