FDA.reportPublic FDA data

OHTrust Nano Ion Water

Manufacturer
Nanoplus Limited (Cayman) Taiwan Branch
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:16:23

Label at a glance#

ProductOHTrust Nano Ion Water
Active ingredientPOTASSIUM HYDROXIDE
Label structure10 sections

Dosage and administration

Spray on hands, skin, or places that need to reduce bacteria. After spray, let it dry and no need to rinse.

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Nano Water hydroxide ions (0.5%) Potassium 0.1% Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Sanitizer to help decrease bacteria. Hygienic disinfectant especially suited for sanitizing hands, skin or the surface that it needs.

Warnings

WARNINGS SECTION

For external use only. Cannot drink

Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Keep out of reach of children

Do not swallow. In case of accidental ingestion, seek professional assistance.

Store at room temperature

OTC - WHEN USING SECTION

For external use only. Cannot drink

Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Keep out of reach of children. Do not swallow. In case of accidental ingestion, seek professional assistance.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not swallow. In case of accidental ingestion, seek professional assistance.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray on hands, skin, or places that need to reduce bacteria. After spray, let it dry and no need to rinse.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Pure Water 99.9%, gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display PanelPrincipal Display PanelPrincipal Display Panel20,000 mL NDC:70970-002-20

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
70970-00270970-002-20

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
GELATIN, UNSPECIFIED2G86QN327LIACT
POTASSIUM HYDROXIDEWZH3C48M4TACTIB
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
d73bf646-34a2-4aa7-e053-2995a90a1d09a60d66c9-3591-3ebe-e053-2995a90af1dd2022-02-04WarningsExact identifier
spl set id: a60d66c9-3591-3ebe-e053-2995a90af1dd

Reported adverse events (FAERS/openFDA)#

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