Zoviro

Manufacturer
Zoviro, LLC
Effective date
2026-09-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-23 00:00:39

Label at a glance#

ProductZoviro
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Water, Carbomer, Glycerin, Aminomethyl propanol, Triethanolamine, Isopropyl myristate, locopheryl acetate, Panthenol, Aloe barbaden-sis leaf extact, Benzophenone-4, Fragrance

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
Place enough product in your palm then rub hands until dry.
Children under 6 years of age should be supervised when using this product.

INDICATIONS & USAGE SECTION

Uses

To reduce bacteria on the skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130383814000085GTIN-13: 0383814000085
EAN-13: 0383814000085
GTIN-12: 383814000085
UPC-A: 383814000085
GTIN storage (14 digits): 00383814000085
Zoviro Hand Sanitizer Soothing Gel 2 fl oz.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83814-00583814-005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-06full-release2026-06-01 01:37:56
22025-02-03full-release2026-06-01 00:54:16

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
40844d7d-3a4d-ce94-e063-6294a90a7fa70e85fb58-7cca-8ae3-e063-6294a90a25532025-10-06WarningsExact identifier
spl set id: 0e85fb58-7cca-8ae3-e063-6294a90a2553

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.