Banobagi Anti-oxidantInjection Mask

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 Anti-oxidantInjection Mask
Active ingredientADENOSINE, GLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

adenosine

INACTIVE INGREDIENT SECTION

Water, Methylpropanediol, Glycerin, Caprylic/Capric Triglyceride, Hydrolyzed Collagen, Centella Asiatica Extract, Bambusa Vulgaris Water, Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Thioctic Acid, Hydroxypropyl Cyclodextrin, Tremella Fuciformis (Mushroom) Extract, Pseudoalteromonas Ferment Extract, Hydrolyzed Wheat Protein, Hydrolyzed Soy Protein, Tripeptide-10 Citrulline, Tripeptide-1, Lecithin, Dimethicone, Polysorbate 60, Xanthan Gum, Tocopheryl Acetate, Sorbitan Sesquioleate, Allantoin, Panthenol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Carbomer, Adenosine, Potassium Hydroxide, 1,2-Hexanediol, Hydroxyacetophenone, Disodium EDTA, Fragrance

OTC - PURPOSE SECTION

Anti-wrinkle, Anti-oxidant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

1. After cleansing your face, gently wipe it out with toner

2. Take the product out of the pouch and adhere it evenly over your face.

3. Remove it after 10~20 minutes.

4. Let the skin absorb the remaining essence by gently patting the skin

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

4. Avoid the use of eye area

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
72001-0018-12022-01-11C16284748780-1ab0e2407-2cd0-f274-e053-dbdaa90a6471Drug Facts
72001-0018-12020-09-27C16284748780-1ab0e2407-2cd0-f274-e053-dbdaa90a6471Drug Facts
72001-0018-12020-09-25C16284748780-1ab0e2407-2cd0-f274-e053-dbdaa90a6471Drug Facts
72001-0018-12020-07-22C16284748780-1ab0e2407-2cd0-f274-e053-dbdaa90a6471Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72001-001872001-0018-1

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
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
d554e8b9-72c2-6576-e053-2a95a90a3d90807e9934-69bf-5e1b-e053-2991aa0a974d2022-01-11WarningsExact identifier
spl id: d554e8b9-72c2-6576-e053-2a95a90a3d90
spl set id: 807e9934-69bf-5e1b-e053-2991aa0a974d

Reported adverse events (FAERS/openFDA)#

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