CELGEN PEARL MOISTURE Solution

Manufacturer
BBHC CO., LTD | STC Nara Co., Ltd
Effective date
2023-04-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:33:08

Label at a glance#

ProductCELGEN PEARL MOISTURE Solution
Active ingredientADENOSINE, NIACINAMIDE
Label structure9 sections

Indications and uses

• Helps improve skin brightness and wrinkle care. • Helps moisturize dehydrated skin.

Dosage and administration

Spray to cover the full facial area and gently tap with fingertips. Use this product in the morning and at night after washing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Niacinamide (2.00%)

Adenosine (0.04%)

Purpose

OTC - PURPOSE SECTION

Skin Brightening

Anti wrinkle

Uses

DOSAGE & ADMINISTRATION SECTION

• Helps improve skin brightness and wrinkle care.

• Helps moisturize dehydrated skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

rash occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If porducts is swallowed, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

Spray to cover the full facial area and gently tap with fingertips. Use this product in the morning and at night after washing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, PEG-60 Hydrogenated Castor Oil, 1,2-Hexanediol, Caprylyl Glycol, Oryzanol, Caprylhydroxamic Acid, Propanediol, Stearic Acid, Cetyl Ethylhexanoate, Beeswax, Disodium EDTA, Citric Acid, Cetearyl Alcohol, Sodium Citrate, Sodium Hyaluronate, Ethylhexylglycerin, Geranium Maculatum Extract, Sodium Chloride, Glucose

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

125ml NDC: 76731-205-01 Label125ml NDC: 76731-205-01 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76731-205-012022-12-30C16284748780-1e4f33bdf-a1d2-d8a0-e053-dadaa90a6e4e76731-205
76731-205-012022-07-29C16284748780-1e4f33bdf-a1d2-d8a0-e053-dadaa90a6e4e76731-205

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76731-20576731-205-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
fbb59f98-5e03-0fdc-e053-6394a90a5ad1ae622d94-36ab-38b5-e053-2995a90a0a222023-05-15WarningsExact identifier
spl set id: ae622d94-36ab-38b5-e053-2995a90a0a22

Reported adverse events (FAERS/openFDA)#

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