Bd E-z Scrub
Chloroxylenol
Becton Dickinson And Company
Human Otc Drug
NDC 17271-502Bd E-z Scrub also known as Chloroxylenol is a human otc drug labeled by 'Becton Dickinson And Company'. National Drug Code (NDC) number for Bd E-z Scrub is 17271-502. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Bd E-z Scrub drug includes Chloroxylenol - 30 mg/mL . The currest status of Bd E-z Scrub drug is Active.
Drug Information:
| Drug NDC: | 17271-502 |
| 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: | Bd E-z 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: | Chloroxylenol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Becton Dickinson And Company |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Solution |
| 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: | CHLOROXYLENOL - 30 mg/mL
|
| 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: | 01 Apr, 2000 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 07 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. |
| 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: | Becton Dickinson and Company
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1245176
1245181
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 0F32U78V2Q
|
| 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 |
|---|
| 17271-502-01 | 6 BOTTLE in 1 BOX (17271-502-01) / 946 mL in 1 BOTTLE | 01 Apr, 2000 | 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 antiseptic
Product Elements:
Bd e-z scrub chloroxylenol aloe vera leaf sodium cocoyl isethionate disodium laureth sulfosuccinate fd&c green no. 3 d&c yellow no. 10 lanolin sodium laureth-3 sulfate poloxamer 184 propylene glycol water chloroxylenol chloroxylenol
Indications and Usage:
Uses surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care cleaning of healthcare personnel hands: helps reduce bacteria that potentially can cause disease
Warnings:
Warnings for external use only do not use if redness or irritation occurs when using this product avoid contact with eyes stop use and ask a doctor if severe adverse reactions occur keep out of reach of children. if swallowed or gets in eyes, get medical help or contact a poison control center right away.
Do Not Use:
Warnings for external use only do not use if redness or irritation occurs when using this product avoid contact with eyes stop use and ask a doctor if severe adverse reactions occur keep out of reach of children. if swallowed or gets in eyes, get medical help or contact a poison control center right away.
When Using:
When using this product avoid contact with eyes
Dosage and Administration:
Directions surgical hand scrub wet hands and forearms with water scrub with a wet brush for 3 minutes with 5 ml pcmx foam solution scrub all planes of each hand and both forearms a separate nail cleaner may be used rinse thoroughly with running water wash for an additional 3 minutes with 5 ml pcmx foam solution rinse thoroughly with running water health care personnel hand wash wet hands with water dispense about 5 ml of solution into cupped hands wash in a vigorous manner for 30 seconds rinse thoroughly with running water
Stop Use:
Stop use and ask a doctor if severe adverse reactions occur
Package Label Principal Display Panel:
Principal display panel â bottle label bd e-z scrub⢠3% chloroxylenol antiseptic solution ref 372404 ⢠ndc 17271-502-01 foreign patents and patents pending. u.s. patents 6,053,369 - 6,308,866 32 fl. oz (946 ml) 3% pcmx principal display panel â bottle label
Further Questions:
Questions? 1-800-453-4538 monday to friday, 8 a.m. to 5 p.m. mst