FDA.reportPublic FDA data

dAlba Vegan Tone-Up Sunscreen

Manufacturer
ADMTMAX LLC | Kolmar Korea Co., Ltd
Effective date
2024-08-27
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 Tone-Up Sunscreen
Active ingredientHOMOSALATE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosagedosage

WARNINGS SECTION

warningwarning

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INDICATIONS & USAGE SECTION

indicationindication

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

children out of reachchildren out of reach

OTC - PURPOSE SECTION

purposepurpose

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Main DisplayMain Display

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84662-040-03dAlba Vegan Tone-Up Sunscreen50 mL in 1 TUBECREAM502

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
84662-04084662-040-03

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
1,3-PROPANEDIOL BIS(4-AMINOBENZOATE)8860R9ORQRIACT
HOMOSALATEV06SV4M95SACTIB

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 Tone-Up SunscreenHOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDEADMTMAX LLC20adebef-2841-a5c2-e063-6394a90ab0632024-08-27WarningsExact identifier
ndc (package): 84662-040-03
ndc (product): 84662-040
ndc11 (package): 84662004003
spl id: 20ae7cb4-d118-0901-e063-6394a90aa7fc
spl set id: 20adebef-2841-a5c2-e063-6394a90ab063

Reported adverse events (FAERS/openFDA)#

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