Banobagi Milk Thistle Repair Serum

Manufacturer
Banobagi Co., Ltd.
Effective date
2022-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:18:08

Label at a glance#

ProductBanobagi Milk Thistle Repair Serum
Active ingredientNIACINAMIDE, ADENOSINE, GLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

niacinamide, adenosine

INACTIVE INGREDIENT SECTION

Arctium Lappa Root Extract, Glycerin, 1,2-Hexanediol, Dipropylene Glycol, Butylene Glycol, Diethoxyethyl Succinate, Betaine, Silybum Marianum Seed Extract, Centella Asiatica Extract, Madecassoside, Echium Plantagineum Seed Oil, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Acetyl Hexapeptide-8, Copper Tripeptide-1, Panthenol, Ethylhexylglycerin, Disodium EDTA, Hydroxyacetophenone, Water, Xanthan Gum, Carbomer, Hydrogenated Lecithin, Octyldodeceth-16, Tromethamine, Octyldodecanol, Tocopherol

OTC - PURPOSE SECTION

Brightening, , Anti-wrinkle, Repair, Recovery

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Balance the skin with toner after cleansing and use several drops and spread evenly on your face. Apply one more time at the area you want to make it more healthy.

WARNINGS SECTION

1. If abnormal symptoms or side effects such as red spots, swelling, or itching are present in the cosmetics or in the direct sunlight after use, consult a specialist

2. Do not use in wounded areas

3. Precautions for storage and handling

- Keep out of reach of children

- Keep away from direct sunlight

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72001-0016-12022-01-11C16284748780-1ab0e2407-269f-f274-e053-dbdaa90a6471Drug Facts
72001-0016-12020-09-27C16284748780-1ab0e2407-269f-f274-e053-dbdaa90a6471Drug Facts
72001-0016-12020-09-25C16284748780-1ab0e2407-269f-f274-e053-dbdaa90a6471Drug Facts
72001-0016-12020-07-22C16284748780-1ab0e2407-269f-f274-e053-dbdaa90a6471Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72001-001672001-0016-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
ADENOSINEK72T3FS567ACTIB
GLYCERINPDC6A3C0OXACTIB
WATER059QF0KO0RIACT

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
d554de0b-2a4b-87b1-e053-2a95a90a23a8807e9934-6872-5e1b-e053-2991aa0a974d2022-01-11WarningsExact identifier
spl id: d554de0b-2a4b-87b1-e053-2a95a90a23a8
spl set id: 807e9934-6872-5e1b-e053-2991aa0a974d

Reported adverse events (FAERS/openFDA)#

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