Clorox Hand Sanitizer
Benzalkonium Chloride
Brand Buzz Llc
Human Otc Drug
NDC 69540-0036Clorox Hand Sanitizer also known as Benzalkonium Chloride is a human otc drug labeled by 'Brand Buzz Llc'. National Drug Code (NDC) number for Clorox Hand Sanitizer is 69540-0036. This drug is available in dosage form of Cloth. The names of the active, medicinal ingredients in Clorox Hand Sanitizer drug includes Benzalkonium Chloride - .13 g/100g . The currest status of Clorox Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 69540-0036 |
| 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: | Clorox Hand Sanitizer |
| 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: | Brand Buzz Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cloth |
| 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 - .13 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: | 24 Aug, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 08 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: | Brand Buzz LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1038558
|
| 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 |
|---|
| 69540-0036-1 | 20 PATCH in 1 POUCH (69540-0036-1) / .13 g in 1 PATCH | 24 Aug, 2021 | N/A | No |
| 69540-0036-2 | 40 PATCH in 1 CANISTER (69540-0036-2) / .13 g in 1 PATCH | 24 Aug, 2021 | N/A | No |
| 69540-0036-3 | 100 PATCH in 1 CANISTER (69540-0036-3) / .13 g in 1 PATCH | 24 Aug, 2021 | N/A | No |
| 69540-0036-4 | 270 PATCH in 1 CANISTER (69540-0036-4) / .13 g in 1 PATCH | 24 Aug, 2021 | 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 antimicrobial
Product Elements:
Clorox hand sanitizer benzalkonium chloride aloe vera leaf peg-75 lanolin quaternium-52 peg-8 dimethicone disodium cocoamphodiacetate matricaria chamomilla flowering top phenoxyethanol potassium sorbate cetylpyridinium chloride sodium benzoate citric acid monohydrate water benzalkonium chloride benzalkonium
Indications and Usage:
Uses hand sanitizing to help reduce bacteria on the skin.
Warnings:
Warnings for external use only. when using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. discontinue use if irritation and redness develop. if condition persists for more than 72 hours, consult a physician. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away
When Using:
When using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. discontinue use if irritation and redness develop. if condition persists for more than 72 hours, consult a physician.
Dosage and Administration:
Directions wet hands thoroughly with product and allow to dry.
Package Label Principal Display Panel:
Clorox pro⢠clorox⢠hand sanitizing wipes kills 99.99% germs* cleans hands bleach-free cloroxpro⢠hand sanitizing wipes kill 99.99% of mopst illness causing germs, so you can clean your hands with confidence. *kills 99.99% of most illness causing germs wipe dimensions: 5.75in. x 7.5in. (14.6 cm x 19 cm) remove lid by lifting upward. pull wipe from center of the roll and thread through the underside of lid. do not put finger through the hole. close lid and pull wipe from canister at an angle. snap lid cap shut to retain moisture. to dispose: place in waste basket after use. do not flush developed in usa | responsibly made in china ©2021 distributed by brand buzz llc., 1407 broadway, new york, ny 10018 clorox and other trademarks are used by brand buzz llc under license from the clorox company or its affiliates. 20 wipes 40 wipes 100 wipes 270 wipes 20 40 100 270
Further Questions:
Questions of comments? visit us at www.brandbuzzcp.com or call us at 1-888-508-4750