NDC 75430-002 Acid Oxidation Potential Water Disinfection Wet Towel

Acid Oxidation Potential Water Disinfection Wet Towel

NDC Product Code 75430-002

NDC CODE: 75430-002

Proprietary Name: Acid Oxidation Potential Water Disinfection Wet Towel What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Acid Oxidation Potential Water Disinfection Wet Towel What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 75430-002-01

Package Description: 6 g in 1 BAG

NDC 75430-002-02

Package Description: 60 g in 1 BAG

NDC 75430-002-03

Package Description: 120 g in 1 BAG

NDC 75430-002-04

Package Description: 180 g in 1 BAG

NDC 75430-002-05

Package Description: 240 g in 1 BAG

NDC 75430-002-06

Package Description: 300 g in 1 BAG

NDC 75430-002-07

Package Description: 360 g in 1 BAG

NDC 75430-002-08

Package Description: 420 g in 1 BAG

NDC 75430-002-09

Package Description: 480 g in 1 BAG

NDC 75430-002-10

Package Description: 540 g in 1 BAG

NDC 75430-002-11

Package Description: 600 g in 1 BAG

NDC Product Information

Acid Oxidation Potential Water Disinfection Wet Towel with NDC 75430-002 is a a human over the counter drug product labeled by Fuzhou Meimei Environmental Protection Technology Co.,ltd.. The generic name of Acid Oxidation Potential Water Disinfection Wet Towel is acid oxidation potential water disinfection wet towel. The product's dosage form is patch and is administered via topical form.

Labeler Name: Fuzhou Meimei Environmental Protection Technology Co.,ltd.

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Acid Oxidation Potential Water Disinfection Wet Towel Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYPOCHLOROUS ACID .9 g/100g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Fuzhou Meimei Environmental Protection Technology Co.,ltd.
Labeler Code: 75430
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 05-06-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Acid Oxidation Potential Water Disinfection Wet Towel Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingerdient

Available chlorine 0.9%

Purpose

Disinfect

Uses

Sanitary and surgical hand disinfection,object surface disinfection;

Warnings

Store in a cool ,dry placeAvoid 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 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.

Other Information

Physical indicators:Orp≥1100mv, ph value 2-3Store between 15-30C(59-86F)Avoid freezing and excessive heat above 40C(104F)

Inactive Ingredients

Purified water, Nonwoven fabric

* Please review the disclaimer below.