FDA.reportPublic FDA data

Ivresse Sanitizer Disinfectant Spray

Manufacturer
Ivresse Internacional, S.A. de C.V.
Effective date
2023-09-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:26:10

Label at a glance#

ProductIvresse Sanitizer Disinfectant
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Spray onto hands at maximun distance of 6 inches. Wet hands thoroughly with product and rub hands together until dry. Do not spray onto face.  Avoid breathing mist and use in well ventilated area.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 94% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product:

OTC - WHEN USING SECTION

  • Do not use in the eyes. Rinse with water to remove.
  • Do not puncture or incinerate. Contents under pressure.

Stop use and ask a doctor 

OTC - STOP USE SECTION

If irritation or redness develop and last more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray onto hands at maximun distance of 6 inches.
  • Wet hands thoroughly with product and rub hands together until dry.
  • Do not spray onto face. 
  • Avoid breathing mist and use in well ventilated area.

Other Information

SPL UNCLASSIFIED SECTION

  • Do not store above 120 °F
  • May stain some fabrics.
  • Not for use on hard surface. Harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Surfactants, Citrus scent, Propellant gas.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78740-00478740-004-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BERACTANTS866O45PIGIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
053eb0b1-d021-a9d2-e063-6294a90a4182acafb8d9-06b1-ebd1-e053-2a95a90ad6402023-09-13WarningsExact identifier
spl id: 053eb0b1-d021-a9d2-e063-6294a90a4182
spl set id: acafb8d9-06b1-ebd1-e053-2a95a90ad640

Reported adverse events (FAERS/openFDA)#

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