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Clorox antimicrobial - Medication Information

Product NDC Code 69540-0031
Drug Name

Clorox antimicrobial

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1046593
Application Number part333A
Labeler Name Brand Buzz LLC
Packages
Package NDC Code Description
69540-0031-1 650 ml in 1 bottle, plastic (69540-0031-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzalkonium Chloride 0.13%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Apply onto wet hands, lather for 30 seconds and rinse thoroughly.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Sodium Laureth Sulfate, Sodium Chlroride, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Laureth-3, Sodium Bicarbonate, Disodium EDTA, Fragrance, Methylchloroisothiazolinone, Methylisothiazoline, Blue 1 (Ci 42090), Red 33 (Ci 17200).

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use For handwashing to decrease bacteria on skin

Purpose

Information about the drug product’s indications for use.
Purpose Antibacterial

Spl product data elements

Usually a list of ingredients in a drug product.
Clorox Antimicrobial Benzalkonium Chloride SODIUM LAURETH SULFATE SODIUM CHLORIDE SODIUM C14-16 OLEFIN SULFONATE COCAMIDOPROPYL BETAINE C12-14 PARETH-12 EDETATE DISODIUM ANHYDROUS SODIUM BICARBONATE METHYLCHLOROISOTHIAZOLINONE WATER FD&C BLUE NO. 1 D&C RED NO. 33 BENZALKONIUM CHLORIDE BENZALKONIUM Lavender

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Clorox Antimicrobial HandSoap Ultra Concentrated Dishwashing Liquid Lavender Scent with Oxi Bleach-Free 8FL OZ (0.5 PT) 236 mL Label Label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information Avoid freezing and excessive heat above 40℃ (104℉). Do not add bleach. Not for use in dishwashers. PHOSPATE-FREE BLEACH-FREE Distributed by: Brand Buzz LLC., 1407 Broadway, New York, NY 10018 Clorox and logo are registered trademarks of the Clorox Company and are used under license by Brand Buzz LLC. All Rights Reserved.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments? Visit us at www.brandbuzzcp.com or call us at: 1-888-508-4750 For more product ingredient information, visit www.brandbuzzcp.com/ingredients

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water. If irritation persists, contact a Poison Control Center right away. Keep out of reach of children.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API