Ido Disinfection Tissue
Isopropyl Alcohol
Ido Pharm
Human Otc Drug
NDC 77039-021Ido Disinfection Tissue also known as Isopropyl Alcohol is a human otc drug labeled by 'Ido Pharm'. National Drug Code (NDC) number for Ido Disinfection Tissue is 77039-021. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ido Disinfection Tissue drug includes Isopropyl Alcohol - 83 mL/100g . The currest status of Ido Disinfection Tissue drug is Active.
Drug Information:
| Drug NDC: | 77039-021 |
| 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: | Ido Disinfection Tissue |
| 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: | Isopropyl Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Ido Pharm |
| 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: | ISOPROPYL ALCOHOL - 83 mL/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: | 02 Jun, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 10 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: | IDO PHARM
|
| 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: | ND2M416302
|
| 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 |
|---|
| 77039-021-01 | 760 g in 1 PACKAGE (77039-021-01) | 02 Jun, 2022 | 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:
â disinfection of hands and skin, disinfection of surgical site skin â disinfectant tissue that can be used in various ways at home, school, restaurant, and toilet
Product Elements:
Ido disinfection tissue isopropyl alcohol water isopropyl alcohol isopropyl alcohol
Indications and Usage:
â take out a tissue one at a time and wipe the area that needs disinfection. â close the cap after use â supervise children under 6 years of age when using this product to avoid swallowing
Warnings:
â observe the indicated usage and standard usage. â be careful not to let the contents come into contact with your eyes. â do not inhale or drink the contents. â when using in an enclosed space, provide sufficient ventilation. â keep away from fire or heat. â keep out of reach of children. â if the contents get into your eyes, rinse with clean water and consult a doctor if there are any abnormalities. â if the contents are eaten or swallowed, take first aid and consult a doctor immediately.
Dosage and Administration:
Topical use only
Package Label Principal Display Panel:
Label