Zoviro | FunFoxMeds

Zoviro BENZALKONIUM CHLORIDE ZOVIRO, LLC FDA Approved Use Hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Generic: BENZALKONIUM CHLORIDE

Mfr: ZOVIRO, LLC FDA OTC

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Substance Benzalkonium Chloride

Route

TOPICAL

Applications

505G(A)(3)

Product NDC

83814-0004-00 83814-0004-01

Package NDC

83814-004-01

Drug Facts

Composition & Profile

Active Ingredients

Active ingredient Benzalkonium chloride 0.13%

Inactive Ingredients

Inactive ingredients Water Glycerin Ethylhexylglycerin Phenoxyethanol Propylene Glycol Fragrance Aloe Barbadensis Leaf Extract Citrus Aurantium Bergamia (Bergamot) Fruit Oil Citrus Aurantium Dulcis (Orange) Oil

Strengths

0.13 %

Treats Conditions

Use Hand Sanitizing To Decrease Bacteria On The Skin Recommended For Repeated Use

Identifiers & Packaging

Container Type UNKNOWN

NDC 83814-0004-00

All Product Codes

83814-0004-00 83814-0004-01

UPC

0383814000016

UNII

F5UM2KM3W7

SPL Set IDs

0e2b4917-0422-b320-e063-6394a90a731b

Packaging

Label

Package Descriptions

Label

Overview

Use Hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Indications & Usage

Use Hand sanitizing to decrease bacteria 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 & Precautions

Warnings For external use only

Purpose

Purpose Antiseptic

When Using

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop Use & Ask a Doctor

Stop use and ask a doctor if imtaton or redness develops, or if condition 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.

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Additional Information

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# Zoviro

## About this page

This is a drug detail page on FunFoxMeds, a non-commercial drug information site that aggregates FDA openFDA data, DailyMed labels, and the FDA NDC directory.
It shows the prescribing information, ingredients, and identifiers for Zoviro. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** Zoviro
- **Brand names:** ZOVIRO
- **Generic names:** BENZALKONIUM CHLORIDE
- **Manufacturers:** ZOVIRO, LLC
- **Active substances:** Benzalkonium Chloride
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Strengths:** 0.13 %
- **Routes of administration:** TOPICAL
- **Active ingredients:** Active ingredient Benzalkonium chloride 0.13%
- **Inactive ingredients:** 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 & use

- **Treats:** Use Hand Sanitizing To Decrease Bacteria On The Skin Recommended For Repeated Use
**Purpose:** Purpose Antiseptic
**Overview:** Use Hand sanitizing to decrease bacteria on the skin Recommended for repeated use
**Indications:** Use Hand sanitizing to decrease bacteria 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 & safety

**Warnings:** Warnings For external use only
**When using:** When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
**Stop use and ask a doctor:** Stop use and ask a doctor if imtaton or redness develops, or if condition 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.

## Storage & packaging

- **Container type:** UNKNOWN
- **Primary NDC:** 83814-0004-00
- **NDCs:** 83814-0004-00, 83814-0004-01
- **Package NDCs:** 83814-004-01
- **UPCs:** 0383814000016
- **Package descriptions:** Label

## Identifiers

- **FDA application numbers:** 505G(A)(3)
- **SPL set IDs:** 0e2b4917-0422-b320-e063-6394a90a731b
- **Product codes:** 83814-0004-00, 83814-0004-01
- **UNIIs:** F5UM2KM3W7

## Data sources

- **Provenance:** openFDA (FDA NDC directory, FDA drug labels) and DailyMed.
- **Disclaimer:** This page is not medical advice. Always consult a licensed healthcare provider for medical decisions.