FDA.reportPublic FDA data

dAlba Vegan Mild Sunscreen

Manufacturer
ADMTMAX LLC | Kolmar Korea Co., Ltd
Effective date
2025-06-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:02:36

Label at a glance#

ProductdAlba Vegan Mild Sunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

warningwarning

DOSAGE & ADMINISTRATION SECTION

dosagedosage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

out of reach childrenout of reach children

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredients

OTC - PURPOSE SECTION

purposepurpose

INDICATIONS & USAGE SECTION

indicationindication

WARNINGS SECTION

warningswarnings

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Main DisplayMain Display

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84662-030-02dAlba Vegan Mild Sunscreen50 mL in 1 TUBECREAM503

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84662-03084662-030-02

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
ISODODECANEA8289P68Y2IACT
ZINC OXIDESOI2LOH54ZACTIB

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 Mild SunscreenZINC OXIDEADMTMAX LLC20ab5698-cd9f-0821-e063-6394a90a60d72025-06-08WarningsExact identifier
ndc (package): 84662-030-02
ndc (product): 84662-030
ndc11 (package): 84662003002
spl id: 371bc066-2b28-6ea0-e063-6394a90aa871
spl set id: 20ab5698-cd9f-0821-e063-6394a90a60d7

Reported adverse events (FAERS/openFDA)#

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