Ohtrust Nano Ion Water
Hydroxide Ions
Nanoplus Life Biomedical Technology Co. Ltd.
Human Otc Drug
NDC 70970-006Ohtrust Nano Ion Water also known as Hydroxide Ions is a human otc drug labeled by 'Nanoplus Life Biomedical Technology Co. Ltd.'. National Drug Code (NDC) number for Ohtrust Nano Ion Water is 70970-006. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ohtrust Nano Ion Water drug includes Hydroxide Ion - .2 g/100mL . The currest status of Ohtrust Nano Ion Water drug is Active.
Drug Information:
| Drug NDC: | 70970-006 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Ohtrust Nano Ion Water |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Hydroxide Ions |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Nanoplus Life Biomedical Technology Co. Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | HYDROXIDE ION - .2 g/100mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 23 Nov, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 May, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Nanoplus Life Biomedical Technology Co. Ltd.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 9159UV381P
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 70970-006-01 | 60 mL in 1 BOTTLE, SPRAY (70970-006-01) | 23 Nov, 2020 | N/A | No |
| 70970-006-02 | 1000 mL in 1 BOTTLE, PUMP (70970-006-02) | 23 Nov, 2020 | N/A | No |
| 70970-006-03 | 5000 mL in 1 BOTTLE, PLASTIC (70970-006-03) | 23 Nov, 2020 | N/A | No |
| 70970-006-04 | 20000 mL in 1 PAIL (70970-006-04) | 23 Nov, 2020 | N/A | No |
| 70970-006-05 | 1000 mL in 1 BOTTLE, PLASTIC (70970-006-05) | 23 Nov, 2020 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose anti-bacterial, anti-viral
Product Elements:
Ohtrust nano ion water hydroxide ions water hydroxide ion hydroxide ion
Indications and Usage:
Use sanitizer to help decrease bacteria. hygienic disinfectant especially suited for sanitizing hands, skin, or the surface that it needs.
Warnings:
Warnings for external use only. cannot drink
When Using:
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 .
Dosage and Administration:
Directions spray on hands, skin, or places that need to reduce bacteria. after spray, let it dry and no need to rinse.
Package Label Principal Display Panel:
Package label - principal display panel 60 ml ndc: 70970-006-01 1000 ml ndc: 70970-006-02 5000 ml ndc: 70970-006-03 20000 ml ndc: 70970-006-04 60 ml label 1000 ml label 5000 ml label 20000 ml label drug facts label