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Novex anti-bacterial hand sanitizer wipe - Medication Information

Product NDC Code 71734-118
Drug Name

Novex anti-bacterial hand sanitizer wipe

Type Brand
Active Ingredients
Benzalkonium chloride .05 g/100g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 2553300
Application Number M003
Labeler Name JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Packages
Package NDC Code Description
71734-118-01 3.7 g in 1 package (71734-118-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkonium Chloride .......... 0.05 %

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 Adults and children over 2 years: Tear open packet, unfold and use as a wash cloth. Allow hands to dry without wiping.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Water, Propylene glycol, Polysorbate 20, Dipropylene glycol, Ethylhexyl_x0002_glycerin, Chlorphenesin, Bronopol, Citric Acid.

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 personal hand hygiene to help prevent the spread of bacteria.

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.
Novex Anti-Bacterial Hand Sanitizer Wipe benzalkonium chloride WATER PROPYLENE GLYCOL POLYSORBATE 20 DIPROPYLENE GLYCOL CHLORPHENESIN BRONOPOL BENZALKONIUM CHLORIDE BENZALKONIUM

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

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.
For external use only. Do not use in eyes. If this occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.

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. 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 eyes. If this occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours. Keep out of reach of children. 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