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Zogics antibacterial foaming hand - Medication Information

Product NDC Code 72202-201
Drug Name

Zogics antibacterial foaming hand

Type Brand
Active Ingredients
Chloroxylenol 1 g/l
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1941461
Application Number 505G(a)(3)
Labeler Name Zogics, LLC
Packages
Package NDC Code Description
72202-201-41 3.78 l in 1 bottle, plastic (72202-201-41)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT Chloroxylenol 0.1%

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 a small amount, covering hands with product for 30 seconds. Lather and rinse. Children under 6 years of age should be supervised when using this product.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS Sodium C14-16 Olefin Sulfonate, Glycerin, Propylene Glycol, Cocamidopropyl Hydroxysultaine, Sodium Benzoate, Propanediol, Sodium Polyitaconate, 2-Bromo-2-Nitropropane-1,3-Diol, Dibromocyanoacetamide, Methylchloroisothiazolinone, Methylisothiazolinone

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.
USES • Handwash to help decrease bacteria on the skin.

Purpose

Information about the drug product’s indications for use.
PURPOSE Antiseptic Handwashing

Spl product data elements

Usually a list of ingredients in a drug product.
Zogics Antibacterial Foaming Hand Chloroxylenol SODIUM BENZOATE SODIUM C14-16 OLEFIN SULFONATE SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED) PROPYLENE GLYCOL PROPANEDIOL BRONOPOL GLYCERIN DIBROMOCYANOACETAMIDE CHLOROXYLENOL CHLOROXYLENOL METHYLISOTHIAZOLINONE METHYLCHLOROISOTHIAZOLINONE COCAMIDOPROPYL HYDROXYSULTAINE

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.
Principal Display Panel

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Stop use and ask a doctor if irritation or rash appears and lasts

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. If swallowed, get medical help or contact a Poison Control Center right away.

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. Do not use in the eyes. In case of contact, immediately flush eyes with water.

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