FDA.reportPublic FDA data

Harper and Scott 62% Hand Sanitizer Gel Unscented 62% v/v

Manufacturer
Bell International Laboratories, Inc.
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:09

Label at a glance#

Product62% v/v Unscented
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

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

For external use only. Keep away from heat or flame.

Do not use: in children less than 2 months of age or in open skin wounds

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.

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

Place enough product on hand to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product and avoid swallowing.

Other Information

OTC - WHEN USING SECTION

Store between 15-30 C (59-86 F).

Avoid freezing and excessive heat above 40 C (104 F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Hydroxypropyl Guar, Citric Acid, Calendula Officinalis Flower Extract, Chamomilla Recutita Flower Extract, Aloe Barbadensis Leaf Juice

RECENT MAJOR CHANGES SECTION

Corrected the Uses section heading from the incorrect "Inactive ingredient section" to the correct "Indications and Usage Section"

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

back 3 mlback 3 mlfront 3 mlfront 3 ml

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-24576150-245-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GUARAPROLOSE (1300 MPA.S AT 1%)1530WMS90SIACT
CHAMOMILEFGL3685T2XIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
GLYCERINPDC6A3C0OXIACT

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
bba01ed5-739c-1233-e053-2a95a90aa45fa529f811-0089-9ee0-e053-2995a90a13a22021-02-18WarningsExact identifier
spl set id: a529f811-0089-9ee0-e053-2995a90a13a2

Reported adverse events (FAERS/openFDA)#

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