Label: OHTRUST NANO ION WATER- potassium hydroxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70970-002-50 - Packager: Nanoplus Limited (Cayman) Taiwan Branch
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 13, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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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.
Store at room temperature
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WHEN USING
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor
Keep out of reach of children. Do not swallow. In case of accidental ingestion, seek professional assistance.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
OHTRUST NANO ION WATER
potassium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70970-002 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 WATER (UNII: 059QF0KO0R) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70970-002-50 5000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/20/2020 Labeler - Nanoplus Limited (Cayman) Taiwan Branch (656283417) Establishment Name Address ID/FEI Business Operations Nanoplus Limited (Cayman) Taiwan Branch 656283417 manufacture(70970-002)
5000 mL NDC: 70970-002-50