Virocide Antibacterial Wipes
FDA Label NDC 77005-007

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Virocide Llc for the product Virocide Antibacterial Wipes (NDC 77005-007). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - do not use, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings

Warnings
For external use only.

Otc - When Using

When using this product, avoid contact with the eyes.
In case of contact, rinse eyes thoroughly with water.

When using this product do not get
into eyes. If contact occurs, rinse
thoroughly with water.

Otc - Do Not Use

Do not use if you are allergic to any of
the ingredients.

Otc - Stop Use

Stop use and ask a doctor if irritation
or rash develops and continues 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, Aloe Vera (Aloe Barbadensis)
Leaf, Anhydrous Citric Acid,
Dimethicone, Edetate Sodium
Tetrahydrate, Hydantoin,
Polysorbate 20,Tocopheryl Acetate
(Vitamin E), Glycerin, Fragrance,
Methylchloroisothiazolinone,
Methylisothiazolinone.

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