Nanoplus Limited Taiwan 001-06

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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

Summary of Product characteristics

OHTRUST NANO ION WATER- ALCOHOL 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 LIMITED TAIWAN 001-06
ACTIVE INGREDIENT(S)
Nano Water hydroxide ions (0.5%) Potassium 0.1% Purpose: Antimicrobial
PURPOS E
Antimicrobial
US E
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
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. If swallowed, get medical help or
contact a Poison Control Center right
away.
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: 70970-001-06
OHTRUST NANO ION WATER
Nanoplus Limited (Cayman) Taiwan Branch
alcohol liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:70 9 70 -0 0 1
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
PO TASSIUM HYDRO XIDE (UNII: WZH3C48 M4T) (HYDROXIDE ION - UNII:9 159
UV38 1P)
POTASSIUM HYDROXIDE 0 .2 g in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
GELATIN, UNSPECIFIED (UNII: 2G8 6 QN327L)
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:70 9 70 -0 0 1-
0 6
6 0 mL in 1 BOTTLE, SPRAY; Type 0 : No t a Co mbinatio n
Pro duc t
0 5/15/20 20
MARKETING INFORMATION
MARKE TING CATE