Dynarex Povidone Iodine Surgical Scrub
Povidone Iodine Surgical Scrub Solution
Dynarex Corporation
Human Otc Drug
NDC 67777-142Dynarex Povidone Iodine Surgical Scrub also known as Povidone Iodine Surgical Scrub Solution is a human otc drug labeled by 'Dynarex Corporation'. National Drug Code (NDC) number for Dynarex Povidone Iodine Surgical Scrub is 67777-142. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Dynarex Povidone Iodine Surgical Scrub drug includes Povidone-iodine - 100 mg/7.5mL . The currest status of Dynarex Povidone Iodine Surgical Scrub drug is Active.
Drug Information:
| Drug NDC: | 67777-142 |
| 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: | Dynarex Povidone Iodine Surgical Scrub |
| 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: | Povidone Iodine Surgical Scrub Solution |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Dynarex Corporation |
| 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: | POVIDONE-IODINE - 100 mg/7.5mL
|
| 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: | OTC MONOGRAPH NOT FINAL |
| 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: | 08 May, 2018 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 16 Jan, 2025 |
| 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. |
| Application Number: | part333E |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| 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: | Dynarex Corporation
|
| 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. |
| NUI: | N0000175486
M0011640
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | 85H0HZU99M
|
| 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. |
| Pharmacologic Class EPC: | Antiseptic [EPC]
|
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. |
| Pharmacologic Class CS: | Iodine [CS]
|
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 67777-142-51 | 24 BOTTLE in 1 CASE (67777-142-51) / 473 mL in 1 BOTTLE (67777-142-50) | 08 May, 2018 | N/A | No |
| 67777-142-61 | 4 BOTTLE in 1 CASE (67777-142-61) / 3790 mL in 1 BOTTLE (67777-142-60) | 08 May, 2018 | 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 healthcare antiseptic
Product Elements:
Dynarex povidone iodine surgical scrub povidone iodine surgical scrub solution water povidone-iodine iodine sodium phosphate, dibasic, anhydrous hydroxyethyl cellulose (100 mpa.s at 2%) monoethanolamine glycerin
Indications and Usage:
Uses surgical hand scrub which significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care. preoperative skin preparation for the preparation of the skin prior to surgery. helps reduce bacteria that potentially can cause skin infection
Warnings:
Warnings for external use only do not use if allergic to iodine in the eyes stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.
Do Not Use:
Warnings for external use only do not use if allergic to iodine in the eyes stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.
Dosage and Administration:
Directions surgical hand scrub: clean under nails with a nail pick. nails should be maintained with a 1 millimeter free edge. wet hands and forearms. apply 5 milliliters (teaspoonful) or palmful to hands and forearms. scrub thoroughly for five minutes paying particular attention to the nails, cuticles, and interdigital spaces. rinse and repeat scrub. preoperative skin preparation: clean the area. apply product to the operative site prior to surgery.
Stop Use:
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours
Package Label Principal Display Panel:
Labeling 1425
Further Questions:
Questions? 1-888-dynarex