Electrolyzed Oxidizing Water Disinfection Wipes
Fuzhou Meimei Environmental Protection Technology Co.,ltd.
Human Otc Drug
NDC 75430-002Electrolyzed Oxidizing Water Disinfection Wipes is a human otc drug labeled by 'Fuzhou Meimei Environmental Protection Technology Co.,ltd.'. National Drug Code (NDC) number for Electrolyzed Oxidizing Water Disinfection Wipes is 75430-002. This drug is available in dosage form of Cloth. The names of the active, medicinal ingredients in Electrolyzed Oxidizing Water Disinfection Wipes drug includes Hypochlorous Acid - .9 g/100g . The currest status of Electrolyzed Oxidizing Water Disinfection Wipes drug is Active.
Drug Information:
| Drug NDC: | 75430-002 |
| 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: | Electrolyzed Oxidizing Water Disinfection Wipes |
| 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: | Electrolyzed Oxidizing Water Disinfection Wipes |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Fuzhou Meimei Environmental Protection Technology Co.,ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cloth |
| 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: | HYPOCHLOROUS ACID - .9 g/100g
|
| 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: | 06 May, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 23 Jun, 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: | Fuzhou Meimei Environmental Protection 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. |
| UPC: | 6972694570722
|
| UPC stands for Universal Product Code. |
| UNII: | 712K4CDC10
|
| 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 |
|---|
| 75430-002-01 | 1 POUCH in 1 BAG (75430-002-01) / 1 g in 1 POUCH (75430-002-11) | 06 May, 2020 | N/A | No |
| 75430-002-02 | 10 POUCH in 1 BOX (75430-002-02) / 1 g in 1 POUCH (75430-002-12) | 06 May, 2020 | N/A | No |
| 75430-002-03 | 20 POUCH in 1 BOX (75430-002-03) / 1 g in 1 POUCH (75430-002-13) | 06 May, 2020 | N/A | No |
| 75430-002-04 | 30 POUCH in 1 BOX (75430-002-04) / 1 g in 1 POUCH (75430-002-14) | 06 May, 2020 | N/A | No |
| 75430-002-05 | 50 POUCH in 1 BOX (75430-002-05) / 1 g in 1 POUCH (75430-002-15) | 06 May, 2020 | N/A | No |
| 75430-002-06 | 80 POUCH in 1 BOX (75430-002-06) / 1 g in 1 POUCH (75430-002-16) | 06 May, 2020 | N/A | No |
| 75430-002-07 | 100 POUCH in 1 BOX (75430-002-07) / 1 g in 1 POUCH (75430-002-17) | 06 May, 2020 | N/A | No |
| 75430-002-08 | 200 POUCH in 1 BOX (75430-002-08) / 1 g in 1 POUCH (75430-002-18) | 06 May, 2020 | N/A | No |
| 75430-002-09 | 500 POUCH in 1 BOX (75430-002-09) / 1 g in 1 POUCH (75430-002-19) | 06 May, 2020 | N/A | No |
| 75430-002-10 | 1000 POUCH in 1 BOX (75430-002-10) / 1 g in 1 POUCH (75430-002-20) | 06 May, 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 disinfect
Product Elements:
Electrolyzed oxidizing water disinfection wipes electrolyzed oxidizing water disinfection wipes hypochlorous acid hypochlorous acid water
Indications and Usage:
Uses sanitary and surgical hand disinfection,object surface disinfection;
Warnings:
Warnings store in a cool ,dry place avoid direct sunlight; avoid eating by children, please keep out of reach of children wet wipes are insoluble in water ,do not throw them into the toilet
Do Not Use:
Warnings store in a cool ,dry place avoid direct sunlight; avoid eating by children, please keep out of reach of children wet wipes are insoluble in water ,do not throw them into the toilet
When Using:
When using section open the lid and tear off the inner sealing sticker when you use it.you can remove it freely. when not in use , re-tighten the sealing sticker and close the lid to prevent the wipes from drying out.
Dosage and Administration:
Stop Use:
Package Label Principal Display Panel:
Package label - principal display panel 75430-002-07 100pcs 75430-002-08 200pcs 75430-002-03 20pcs 75430-002-09 500pcs 75430-002-04 30pcs 75430-002-10 1000pcs 75430-002-01 1pcs 75430-002-02 10pcs 75430-002-05 50pcs 75430-002-06 80pcs