DIONA CELL ILLUMINATING BOOSTER

Manufacturer
VAATZ CO., LTD. | EYESEL Co., Ltd.
Effective date
2018-09-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:55

Label at a glance#

ProductDIONA CELL ILLUMINATING BOOSTER
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glycerin

INACTIVE INGREDIENT SECTION

WATER, 1,2-HEXANEDIOL, NIACINAMIDE, SQUALANE, SODIUM DNA, ETC.

OTC - PURPOSE SECTION

Skin protectant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply an appropriate amount to skin and absorb it.

WARNINGS SECTION

1) If following symptoms occur after product use, stop using immediately and consult with a specialist: red spots, swelling, itchiness, and other skin irritations. 2) Avoid contact with eyes and open wounds. 3) Keep out of reach of children. 4) Do not store at high/low temperature. 5) Avoid direct sunlight.

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72573-0002-12020-01-31C16284748780-19d75b9d0-bbb1-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72573-0002-1DIONA CELL ILLUMINATING BOOSTER5 mL in 1 VIALLIQUID51
72573-0002-1DIONA CELL ILLUMINATING BOOSTER12 in 1 BOXLIQUID121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72573-0002DIONA CELL ILLUMINATING BOOSTER (GLYCERIN) LIQUID [VAATZ CO., LTD.]1Legacy NDC, 2 package rows20180928_76e5c194-da68-36fb-e053-2a91aa0a2440.zip

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
72573-000272573-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXACTIB

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
76e5c194-da69-36fb-e053-2a91aa0a244076e5c194-da68-36fb-e053-2a91aa0a24402018-09-27WarningsExact identifier
spl id: 76e5c194-da69-36fb-e053-2a91aa0a2440
spl set id: 76e5c194-da68-36fb-e053-2a91aa0a2440

Reported adverse events (FAERS/openFDA)#

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