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Zoviro - Medication Information

Product NDC Code 83814-004
Drug Name

Zoviro

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 1038558
Application Number 505G(a)(3)
Labeler Name Zoviro, LLC
Packages
Package NDC Code Description
83814-004-01 80 pouch in 1 bag (83814-004-01) / 3.136 g in 1 pouch
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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 Rub hands thoroughly with product and allow to dry. Children under 2 years old should ask a doctor before use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Extract,Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Oil

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 Hand sanitizing to decrease bacteria on the 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.
Zoviro Benzalkonium Chloride BENZALKONIUM CHLORIDE BENZALKONIUM ETHYLHEXYLGLYCERIN GLYCERIN PHENOXYETHANOL WATER BERGAMOT OIL ORANGE OIL ALOE VERA LEAF PROPYLENE GLYCOL

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.
Label

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 imtaton or redness develops, or if condition persists for more than 72 hours.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

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

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