OHTrust Nano Ion Water by Nanoplus Limited (Cayman) Taiwan Branch Nanoplus 005-50

OHTrust Nano Ion Water by

Drug Labeling and Warnings

OHTrust Nano Ion Water by is a Otc medication manufactured, distributed, or labeled by Nanoplus Limited (Cayman) Taiwan Branch. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OHTRUST NANO ION WATER- hydroxide ions, potassium liquid 
Nanoplus Limited (Cayman) Taiwan Branch

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Nanoplus 005-50

Active Ingredient(s)

Nano Water hydroxide ions (0.5%) Potassium 0.1%

Purpose

Antimicrobial

Use

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

Warnings

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.

Directions

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

Other information

• Store at room temperature

Inactive ingredients

Pure Water 99.9%, gel

Package Label - Principal Display Panel

5000 mL NDC: 70970-005-50

OHTRUST NANO ION WATER 
hydroxide ions, potassium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70970-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROXIDE ION (UNII: 9159UV381P) (HYDROXIDE ION - UNII:9159UV381P)	HYDROXIDE ION	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70970-005-50	5000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/05/2020	12/15/2021

Labeler - Nanoplus Limited (Cayman) Taiwan Branch (656283417)

Establishment
Name	Address	ID/FEI	Business Operations
Nanoplus Limited (Cayman) Taiwan Branch		656283417	manufacture(70970-005)

Revised: 2/2022

Document Id: d73b50b4-dac0-406d-e053-2995a90a6f44

34390-5

Set id: a74aa9df-6286-1c09-e053-2995a90a9cc2

Version: 6

Effective Time: 20220204