Bellaskin Brightening Contour Essence

Manufacturer
Ajou Medics Co., Ltd
Effective date
2022-04-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:03:28

Label at a glance#

ProductBellaskin Brightening Contour Essence
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredient: niacinamide

INACTIVE INGREDIENT SECTION

inactive ingredient: Water, Glycerin, Butylene Glycol, Beta-Glucan, Cetanol, Caprylic / Capric Triglyceride, Squalane, Cucubita Pepo(Pumpkin) Fruit Extract, Murdania Keisak Extract, Hamamelis Virginiana(Witchhazel) Leaf Extract, Glyceryl Stearate/ PEG-100 Stearate, Dimethicone, Polysorbate-60, Glyceryl Stearate, Collagen, Beeswax, Methyl Paraben, Phenoxy Ethanol, Arginine, Carbomer, Sorbitan Stearate, Allantoin, Fragrance, Ceramide 3, Propyl Paraben, Acetyl Hexapeptide-8, Copper Tripeptide-1,
Dipotassium Glycyrrhizate, Xanthan gum, Tocopheryl Acetate, Sodium Hyaluronate

OTC - PURPOSE SECTION

whitening and brightening the skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply Proper Amount of the essence on the face

WARNINGS SECTION

■ For external use only.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.
■ Keep out of reach of children.
■ Stop use and ask doctor if rash and irritation develops.

DOSAGE & ADMINISTRATION SECTION

wash the skin to be applied

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76340-0007-12022-04-17C16284748780-1d6a99b39-4eba-a426-e053-dadaa90af4c2Drug Facts
76340-0007-12022-01-28C16284748780-1d6a99b39-4eba-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76340-000776340-0007-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
dce5027f-2844-091d-e053-2995a90a5a7b672012ea-8807-6da5-e053-2991aa0ac3222022-04-17WarningsExact identifier
spl id: dce5027f-2844-091d-e053-2995a90a5a7b
spl set id: 672012ea-8807-6da5-e053-2991aa0ac322

Reported adverse events (FAERS/openFDA)#

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