Otc - Active Ingredient
Active ingredient
Benzalkonium chloride 0.13%
Zoviro Swab
FDA Label NDC 83814-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zoviro, Llc for the product Zoviro (NDC 83814-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - when using, otc - stop use, otc - keep out of reach of children, inactive ingredient, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if imtaton or redness develops, or if condition persists for more than 72 hours.
Otc - 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.
Inactive Ingredient
Inactive ingredients
Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Extract,Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Oil
Dosage & Administration
Directions
Rub hands thoroughly with product and allow to dry.
Children under 2 years old should ask a doctor before use.
Indications & Usage
Use
Hand sanitizing to decrease bacteria on the skin
Recommended for repeated use
Warnings
Warnings
For external use only
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