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Renown antibacterial hand - Medication Information

Product NDC Code 18949-051
Drug Name

Renown antibacterial hand

Type Brand
Active Ingredients
Chloroxylenol 3000 mg/l
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 413261
Application Number 505G(a)(3)
Labeler Name HD Supply
Packages
Package NDC Code Description
18949-051-00 3.78 l in 1 bottle (18949-051-00)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Chloroxylenol 0.3% Purpose Antiseptic

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 Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together to produce a thick lather Rinse and repeat

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients DEIONIZED WATER, SODIUM LAURYL ETHER SULFATE, SODIUM CHLORIDE, COCAMIDE MIPA, SODIUM SULFATE, OCEAN BREEZE FRAGRANCE 16295, MAGNESIUM NITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD & C YELLOW #6, D&C RED NO. 33

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 For hand washing to decrease the bacteria on skin. Recommended for repeated use

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Renown Antibacterial Hand CHLOROXYLENOL WATER SODIUM LAURETH-3 SULFATE SODIUM CHLORIDE COCO MONOISOPROPANOLAMIDE SODIUM SULFATE MAGNESIUM NITRATE CITRIC ACID MONOHYDRATE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE FD&C YELLOW NO. 6 D&C RED NO. 33 CHLOROXYLENOL CHLOROXYLENOL

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.
Package Labeling: 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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use in the eyes. In case of contact, flush eyes with water.

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.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours

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, flush eyes with water. Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away.

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