FDA.reportPublic FDA data

Hand Sanitzer

Manufacturer
McConnell labs Inc | McConnell Labs
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:58:07

Label at a glance#

ProductHand Sanitzer
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

​To help reduce bacteria on the skin that potentially can cause disease Reccomended for repeated use

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • ​To help reduce bacteria on the skin that potentially can cause disease
  • Reccomended for repeated use

Warnings

WARNINGS SECTION

For External use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR SECTION

irritation or rash occurs. These may be signs of a serious condition

Keep out of reach of childen

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

  • Store between 15-30C (59-86F)
  • Avoud freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Hydroxypropylcellulose, fragrance (parfum)

Questions?

OTC - QUESTIONS SECTION

Call us at +1 (541) 526-1417

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Display Panel IPA 70Display Panel IPA 70

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73991-69173991-691-08, 73991-691-02, 73991-691-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS OIL2R04ONI662IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
PEPPERMINT OILAV092KU4JHIACT

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
ca52dfb9-fee7-7b7c-e053-2a95a90ac1f0b191dad1-e48c-131c-e053-2a95a90a6daf2021-08-24WarningsExact identifier
spl set id: b191dad1-e48c-131c-e053-2a95a90a6daf

Reported adverse events (FAERS/openFDA)#

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