OHTrust Nano Ion Water

Manufacturer: Nanoplus Limited (Cayman) Taiwan Branch
Effective date: 2016-09-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:47:14

Label at a glance#

ProductOHTrust Nano Ion Water

Active ingredientPotassium hydroxide

Label structure8 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Potassium hydroxide (0.2%)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

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.

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Nano-ion water, Gel, Small clustered floral water

Directions

DOSAGE & ADMINISTRATION SECTION

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

OHTrust Nano Ion Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

nano water

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1811266	potassium hydroxide 0.2 % Topical Spray	PSN	1
1811266	potassium hydroxide 2 MG/ML Topical Spray	SCD	1
1811266	K+ Hydroxide 2 MG/ML Topical Spray	SY	1
1811266	Pot Hydroxide 2 MG/ML Topical Spray	SY	1
1811266	potassium hydroxide 0.2 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70970-100-02	2020-01-31	C162847	48780-1	9d75b9d1-2757-f424-e053-dadaa90a57ce	OHTrust Nano Ion Water

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70970-100-01	OHTrust Nano Ion Water	100 mL in 1 BOTTLE, SPRAY	LIQUID	100		1
70970-100-02	OHTrust Nano Ion Water	1 in 1 PACKAGE	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70970-100	OHTRUST NANO ION WATER (POTASSIUM HYDROXIDE) LIQUID [NANOPLUS LIMITED (CAYMAN) TAIWAN BRANCH]	1	Legacy NDC, 2 package rows	20160927_446842b8-c2cb-496f-a102-2fd6a4474e7d.zip

Products#

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

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

OHTrust Nano Ion Water
Potassium hydroxide
HYDROXIDE ION
water
GELATIN, UNSPECIFIED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70970-100	70970-100-01, 70970-100-02

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
Name	UNII	Kind
Potassium hydroxide	WZH3C48M4T	ACTIB
water	059QF0KO0R	IACT
GELATIN, UNSPECIFIED	2G86QN327L	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
32460e24-386c-4b03-9a6a-9118cc66fdb4			446842b8-c2cb-496f-a102-2fd6a4474e7d	2016-09-26	Warnings	Exact identifier spl id: 32460e24-386c-4b03-9a6a-9118cc66fdb4 spl set id: 446842b8-c2cb-496f-a102-2fd6a4474e7d

Reported adverse events (FAERS/openFDA)#

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