Waterrok fulvic acid

Manufacturer: Waterrok Co., Ltd.
Effective date: 2021-11-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:26:58

Label at a glance#

ProductWaterrok fulvic acid

Active ingredientFULVIC ACID

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

pulvic acid

OTC - PURPOSE SECTION

Diabetes improvement, blood pressure control, anticancer, immunity improvement, skin disease line, antiviral

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Take 3 times a day, 500ml at a time

WARNINGS SECTION

▪ Keep out of reach of children.

▪ Consult your doctor if you are taking any serious medications or have a medical condition.

￭ Store in the refrigerator, avoid direct sunlight

DOSAGE & ADMINISTRATION SECTION

oral use only

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Waterrok fulvic acid
ROK fulvic acid
FULVIC ACID
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82236-0002	82236-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
FULVIC ACID	XII14C5FXV	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d106b5a5-1eb0-5d0a-e053-2995a90a7157			d10657fb-a410-4546-e053-2995a90afb5e	2021-11-17	Warnings	Exact identifier spl id: d106b5a5-1eb0-5d0a-e053-2995a90a7157 spl set id: d10657fb-a410-4546-e053-2995a90afb5e

Reported adverse events (FAERS/openFDA)#

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