Drugplain

Zoviro 70 mL/100mL

ALCOHOL · LIQUID · Zoviro, LLC

No Recall HistoryCurrently in Shortage
Plain English

Zoviro is a liquid containing alcohol at 70 mL/100mL, taken topical. Manufactured by Zoviro, LLC.

Key Facts

Brand Name
Zoviro
Generic Name
ALCOHOL
NDC Code (Product)
83814-005
Manufacturer
Zoviro, LLC
Strength
70 mL/100mL
Dosage Form
LIQUID
Route
TOPICAL
Marketing Status
Application #
505G(a)(3)
Marketing Start
01/09/2024

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

toxicity to various agents5,895 reports
completed suicide5,392 reports
drug abuse5,225 reports
overdose1,869 reports
death1,582 reports
intentional overdose1,523 reports
cardio-respiratory arrest1,339 reports
suicide attempt1,322 reports
somnolence899 reports
drug dependence897 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Use For hand sanitizing to decrease bactera on the skin Recommended for repeated use

Dosage & Administration

Directions Rub hands thoroughly with product and allow to dry. Children under 2 years old should ask a doctor before use

Warnings

Warnings For external use only

Frequently Asked Questions

What is Zoviro used for?

Zoviro contains ALCOHOL. It is a liquid taken topical. Consult your doctor for specific uses.

Is Zoviro a controlled substance?

Zoviro is not classified as a controlled substance by the DEA.

What is the generic name for Zoviro?

The generic name for Zoviro is ALCOHOL. There are 12 other brand versions of ALCOHOL.

What is the NDC code for Zoviro 70 mL/100mL?

The NDC (National Drug Code) for Zoviro 70 mL/100mL is 83814-005, listed by Zoviro, LLC.

Product NDC

83814-005

Package NDC

83814-005-01

Other Alcohol Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)