Hand Sanitizer

Manufacturer
QVI Inc
Effective date
2020-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:59

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Spray directly on hands and rub in throughly. Children under 6 years old should be supervised when using this product. Do not us on children less than 2 months of age.

Storage and handling

Store below 104F (40C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Hand Sanitizer Spray

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame. For External use only. When using this product do not use in mouth, ears, open skin wounds, or eyes. In case of contact, rinse eye thoroughly with water.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds
  • Ears
  • mouth
  • eyes

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray directly on hands and rub in throughly.
  • Children under 6 years old should be supervised when using this product. Do not us on children less than 2 months of age.

Other information

STORAGE AND HANDLING SECTION

  • Store below 104F (40C). May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, purified water USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120mL NDC:74983-120-02 Ethanol CDC VersionEthanol CDC Version ISO CDC VersionISO CDC Version120 mL NDC:74983-120-02

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74983-120-012022-01-28C16284748780-1d6a99b39-a374-a426-e053-dadaa90af4c2a2f30f9a-ffb3-e8ed-e053-2995a90af3b0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74983-120-01Hand Sanitizer120 mL in 1 BOTTLE, SPRAYSPRAY1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74983-120HAND SANITIZER (ALCOHOL) SPRAY [QVI INC]1Legacy NDC, 1 package rows20200426_a2f30f9a-ffb3-e8ed-e053-2995a90af3b0.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74983-12074983-120-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
a2f2fe87-bbf6-ac44-e053-2a95a90a8b41a2f30f9a-ffb3-e8ed-e053-2995a90af3b02020-04-10WarningsExact identifier
spl id: a2f2fe87-bbf6-ac44-e053-2a95a90a8b41
spl set id: a2f30f9a-ffb3-e8ed-e053-2995a90af3b0

Reported adverse events (FAERS/openFDA)#

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