EXODERMA Waterfall Booster

Manufacturer
The Classeum Co., Ltd | The Classeum Co., Ltd.
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:42:42

Label at a glance#

ProductEXODERMA Waterfall Booster
Active ingredientADENOSINE, NIACINAMIDE
Label structure9 sections

Label contents#

Full prescribing information#

RECENT MAJOR CHANGES SECTION

Added a new product

EXODERMA Waterfall Booster

LIQUID

These highlights do not include all the information needed to use. See full prescribing information.

DOSAGE & ADMINISTRATION SECTION

120mL

1ea

Liquid

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.

INDICATIONS & USAGE SECTION

EXODERMA Waterfall Booster

WARNINGS SECTION

Warnings

OTC - PURPOSE SECTION

EXODERMA Waterfall Booster

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

NIACINAMIDE

ADENOSINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EXODERMA Waterfall Booster

EXODERMA WATERFALL BOOSTEREXODERMA WATERFALL BOOSTER

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
83144-755183144-7551-2

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
WATER059QF0KO0RIACT
ADENOSINEK72T3FS567ACTIB
NIACINAMIDE25X51I8RD4ACTIB

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
f06372cf-8c29-c4d0-e053-2a95a90aadc8f02299d9-e752-7f54-e053-2995a90a13f52022-12-21WarningsExact identifier
spl id: f06372cf-8c29-c4d0-e053-2a95a90aadc8
spl set id: f02299d9-e752-7f54-e053-2995a90a13f5

Reported adverse events (FAERS/openFDA)#

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