FDA.reportPublic FDA data

Zoviro Hand Sanitizer Lavender Breeze Gel, 1 fl oz Bottle

Manufacturer
Zoviro, LLC
Effective date
2026-08-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-08-18 02:02:35

Label at a glance#

ProductZoviro
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

To reduce bacteria on the skin.

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 - STOP USE SECTION

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

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.
Not recommended for infants.

HOW SUPPLIED SECTION

Other information

Store below 110°F (43°C).

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aqua/Water, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Lavandula Angustifolia (Lavender) Oil, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Denatonium Benzoate, Eucalyptus Globulus Leaf Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product label 1oz lable1oz lable

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130383814000313GTIN-13: 0383814000313
EAN-13: 0383814000313
GTIN-12: 383814000313
UPC-A: 383814000313
GTIN storage (14 digits): 00383814000313		FDA 1oz label.jpg

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
83814-00783814-007-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
LAVENDER OILZBP1YXW0H8IACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT
EUCALYPTUS OIL2R04ONI662IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-08-10daily-update2026-08-12 01:01:20
32026-08-08daily-update2026-08-11 01:01:15

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
ZoviroALCOHOLZoviro, LLC9c8ca084-8aef-4616-8d51-aaff3eb253432026-08-12WarningsExact identifier
ndc (package): 83814-007-01
ndc (product): 83814-007
ndc11 (package): 83814000701
spl id: 58e64ef9-f435-1cc0-e063-6294a90adef9
spl set id: 9c8ca084-8aef-4616-8d51-aaff3eb25343

Reported adverse events (FAERS/openFDA)#

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