FDA.reportPublic FDA data

BOTOKI V MASK

Manufacturer
FICC Co., Ltd. | GEOSEONGGDS
Effective date
2021-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:45

Label at a glance#

ProductBOTOKI V MASK
Active ingredientADENOSINE
Label structure9 sections

Indications and uses

■ Helps improve wrinkle problem

Dosage and administration

■ Stretch the product sufficiently and adhere to ears. ■ Remove the product after the absorption of thick water gel and massage gently into skin.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ADENOSINE 0.04%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin, Gelatin, Sodium Polyacrylate, Polyvinyl Alcohol, PVP, Tartaric Acid, Aluminum Hydroxide, Green Tea Extract, Tocopherol, Grape Seed Extract, Collagen, Caffeine, Polysorbate 20, Disodium EDTA, Glaucine, Phosphatidylcholine, Hyaluronic Acid, Urea, Menthol, Perfume, Methionyl r-Clostridium, Botulinum, Polypeptide-1, Hexapeptide-40, Sodium Chloride, Disodium Phosphate, Potassium Phosphate

PURPOSE

OTC - PURPOSE SECTION

Anti wrinkle

WARNINGS

WARNINGS SECTION

For external use only
Consult a specialist if there are abnormal symptoms or side effects such as redness, swelling or itchiness due to direct sunlight during or after use.
Avoid using on wounded areas.
Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Uses

INDICATIONS & USAGE SECTION

■ Helps improve wrinkle problem

Directions

DOSAGE & ADMINISTRATION SECTION

■ Stretch the product sufficiently and adhere to ears.
■ Remove the product after the absorption of thick water gel and massage gently into skin.

Other Information

OTHER SAFETY INFORMATION

■ Keep away from direct sunlight.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81647-150-022023-10-16C16284748780-1f386c64a-402d-0266-e053-dadaa90a7c1adf0a3c74-b8e9-4f24-b555-e408f8f9f9d3
81647-150-022023-01-30C16284748780-1f386c64a-402d-0266-e053-dadaa90a7c1adf0a3c74-b8e9-4f24-b555-e408f8f9f9d3

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
81647-15081647-150-01, 81647-150-02

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
ADENOSINEK72T3FS567ACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
Gelatin2G86QN327LIACT

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
d74d4cad-b61e-4016-b903-488577e8e485df0a3c74-b8e9-4f24-b555-e408f8f9f9d32023-10-16WarningsExact identifier
spl set id: df0a3c74-b8e9-4f24-b555-e408f8f9f9d3

Reported adverse events (FAERS/openFDA)#

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