NDC 55090-001 Chlorine Dioxide Air Disinfectant

Chlorine Dioxide Air Disinfectant

NDC Product Code 55090-001

NDC CODE: 55090-001

Proprietary Name: Chlorine Dioxide Air Disinfectant 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: Chlorine Dioxide Air Disinfectant 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

  • 55090 - Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.
    • 55090-001 - Chlorine Dioxide Air Disinfectant

NDC 55090-001-01

Package Description: 6.5 g in 1 BOTTLE

NDC Product Information

Chlorine Dioxide Air Disinfectant with NDC 55090-001 is a a human over the counter drug product labeled by Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.. The generic name of Chlorine Dioxide Air Disinfectant is chlorine dioxide air disinfectant. The product's dosage form is powder and is administered via topical form.

Labeler Name: Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

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.

Chlorine Dioxide Air Disinfectant 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.

  • CHLORINE DIOXIDE 130 mg/6.5g

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.

  • CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
  • SODIUM BISULFATE (UNII: BU8V88OWIQ)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)
  • SODIUM CHLORITE (UNII: G538EBV4VF)

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: Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.
Labeler Code: 55090
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.

Chlorine Dioxide Air Disinfectant Product Label Images

Chlorine Dioxide Air Disinfectant 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

Dosage & Administration

Store in dark, cool, dry,ventilated_ place, do not contact with acid, organic matter, inflammables and other strong reducing agent or storage together

Inactive Ingredient

Anhydrous sodium sulfateCalciun chlorideSodium bisulfate Sodium chlorite

Indications & Usage

Open the box and aluminum foil bag,according to the configuration of 1m/unit enclosed space, the operation time is 1h

Otc - Active Ingredient

Chlorine Dioxide

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Purpose

Disinfection

Sterilization

Warnings

1. External disinfectant should not be taken orally;Keep out of reach of children;

2. Should not be mixed with other disinfectants, alkali or organic matter;

3. This product can bleach,It shall not be used for disinfection of metal articles;

4. Avoid contact with skin and inhalation of high concentration disinfectant;

5. The product should be kept away from fire and heat source;

6. Do not use in wet places such as rain, high temperature and places with long time sun exposure;

7. Do not breathe near the nose or directly;

8. If the. disinfectant accidentally touches. the eyes,rinse with water immediately, or seek medical advice in severe cases.

* Please review the disclaimer below.