Nanoplus Taiwan 003-06

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) (HYDROXIDE ION - UNII:9159UV381P)

Available from:

Nanoplus Limited (Cayman) Taiwan Branch

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

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

Authorization status:

unapproved drug other

Summary of Product characteristics

                                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 TAIWAN 003-06
ACTIVE INGREDIENT(S)
Nano Water hydroxide ions (0.5%) Potassium 0.1% Purpose: Antimicrobial
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.
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
60 mL NDC: 70970-003-06
Nanoplus Limited (Cayman) Taiwan Branch
OHTRUST NANO ION WATER
hydroxide ions, potassium liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:70970-003
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) (HYDROXIDE ION -
UNII:9159UV381P)
POTASSIUM
HYDROXIDE
0.2 g
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:70970-
003-06
60 mL in 1 BOTTLE, SPRAY; Type 0: Not a
Combination Product
05/21/2020
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR 
                                
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