Country: United States
Language: English
Source: NLM (National Library of Medicine)
HYDROXIDE ION (UNII: 9159UV381P) (HYDROXIDE ION - UNII:9159UV381P)
Nanoplus Limited (Cayman) Taiwan Branch
TOPICAL
OTC DRUG
Antimicrobial Sanitizer to help decrease bacteria. Hygienic disinfectant especially suited for sanitizing hands, skin or the surface that it needs.
unapproved drug other
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._ ---------- 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 Nanoplus Limited (Cayman) Taiwan Branch OHTRUST NANO ION WATER hydroxide ions, potassium liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:70970-005 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 LABELER - Nanoplus Limited (Cayman) Taiwan Branch (65 Read the complete document