Banobagi Milk Thistle Repair

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
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, Caprylic/Capric Triglyceride, Glycerin, 1,2-Hexanediol, Hydrogenated Polydecene, Caprylyl Methicone, Vinyl Dimethicone, Dipropylene Glycol, Silybum Marianum Seed Extract, Cetyl Ethylhexanoate, Cetearyl Alcohol, Niacinamide, Cetearyl Olivate, Glyceryl Stearate, Sorbitan Olivate, Squalane, Panthenol, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Copper Tripeptide-1, Madecassoside, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Echium Plantagineum Seed Oil, Sodium Hyaluronate, Adenosine, Stearic Acid, Ammonium Acryloyldimethyltaurate/VP Copolymer, Polyglyceryl-2 Stearate, Hydroxyacetophenone, Octyldodecanol, Stearyl Alcohol, Sodium Polyacryloyldimethyl Taurate, Dimethiconol, Hydrogenated Lecithin, Caprylyl/Capryl Glucoside, Xanthan Gum, Disodium EDTA, Glyceryl Acrylate/Acrylic Acid Copolymer, Ethylhexylglycerin, 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

After cleansing or at the last step of your skin care, use several drops and spread around evenly on your face and gently pat to absorb the cream

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
72001-0017-12022-01-11C16284748780-1ab0e2407-2adf-f274-e053-dbdaa90a6471Drug Facts
72001-0017-12020-09-27C16284748780-1ab0e2407-2adf-f274-e053-dbdaa90a6471Drug Facts
72001-0017-12020-09-25C16284748780-1ab0e2407-2adf-f274-e053-dbdaa90a6471Drug Facts
72001-0017-12020-07-22C16284748780-1ab0e2407-2adf-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
72001-001772001-0017-1

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
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4ACTIB
ADENOSINEK72T3FS567ACTIB
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
d554ef4c-a69f-642f-e053-2995a90a7016807e9934-6881-5e1b-e053-2991aa0a974d2022-01-11WarningsExact identifier
spl id: d554ef4c-a69f-642f-e053-2995a90a7016
spl set id: 807e9934-6881-5e1b-e053-2991aa0a974d

Reported adverse events (FAERS/openFDA)#

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