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

Drug FactsPrincipal Display Panel5000 mL NDC: 70970-005-50

OHTRUST NANO ION WATER 
hydroxide ions, potassium liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70970-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROXIDE ION (UNII: 9159UV381P) (HYDROXIDE ION - UNII:9159UV381P) HYDROXIDE ION0.2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70970-005-505000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/05/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/05/202012/15/2021
Labeler - Nanoplus Limited (Cayman) Taiwan Branch (656283417)
Establishment
NameAddressID/FEIBusiness Operations
Nanoplus Limited (Cayman) Taiwan Branch656283417manufacture(70970-005)

Revised: 2/2022
 

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