Lifeguard Disinfecting Wipes
Benzalkonium Chloride
Zhejiang Saiveroy Cleaning Products Co., Ltd.
Human Otc Drug
NDC 79680-008Lifeguard Disinfecting Wipes also known as Benzalkonium Chloride is a human otc drug labeled by 'Zhejiang Saiveroy Cleaning Products Co., Ltd.'. National Drug Code (NDC) number for Lifeguard Disinfecting Wipes is 79680-008. This drug is available in dosage form of Swab. The names of the active, medicinal ingredients in Lifeguard Disinfecting Wipes drug includes Benzalkonium Chloride - .1 g/100g . The currest status of Lifeguard Disinfecting Wipes drug is Active.
Drug Information:
| Drug NDC: | 79680-008 |
| 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: | Lifeguard Disinfecting Wipes |
| 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: | Benzalkonium Chloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Zhejiang Saiveroy Cleaning Products Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Swab |
| 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: | BENZALKONIUM CHLORIDE - .1 g/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: | 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: | 07 Dec, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 Jun, 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: | part333A |
| 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: | Zhejiang Saiveroy Cleaning Products Co., LTD.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1038856
|
| 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: | F5UM2KM3W7
|
| 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 |
|---|
| 79680-008-01 | 100 POUCH in 1 CANISTER (79680-008-01) / 3.5 g in 1 POUCH | 07 Dec, 2020 | 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:
Lifeguard disinfecting wipes benzalkonium chloride benzalkonium chloride benzalkonium water phenoxyethanol ethylhexylglycerin propylene glycol aloe vera leaf
Indications and Usage:
Use signle use wipes to clean.
Warnings:
Warning general advice: show this safety data sheet to the doctor in the attendance. eye contact: hold eye open and rinse slowly and gently with water for 15-20 minutes. if preset, remove contact lenses after a poison control center or doctor for further treatment advice. skin contact: rinse skin with plenty of water. if irritation persists, call a doctor. inhalation: move a fresh air. if breathing problems develop, call a doctor. ingestion: drink a glassful of water. call a doctor or poison control center. âif swallowed, get medical help or contact a poison contrl center right away.
Dosage and Administration:
Directions for use; instruction, storage and disposal directions for use: it is a violation of federal law to use this product in a manner inconsistent with labeling. not for cleaning or sanitizing skin. do not use as a diaper wipe or for personal cleansing. instructions: before using, open the tab, then take the wipe and pass it through the hole of the bag. wipe the surface and allow one minute contact time. storage and disposal: dispose of wipe in the trash after use. tightly close seal between uses to retain moisture. please empty container for recycling. if recycling not available, discard container in trash.
Package Label Principal Display Panel:
Label image