Hand Sanitizer

Manufacturer
Durham Distillery
Effective date
2020-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:37:50

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

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#

Do Not Use

OTC - DO NOT USE SECTION

• in children less than 2 months of age

• on open skin wounds

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.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Stop Use and Ask a Doctor

OTC - STOP USE SECTION

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

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.

Other information

OTHER SAFETY INFORMATION

• Store between 15-30C (59-86F)

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

Warnings

WARNINGS AND PRECAUTIONS SECTION

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

Directions

INSTRUCTIONS FOR USE 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

When using this product

WARNINGS SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

Back LabelBack Label

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front labelFront label

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74016-000174016-0001-1, 74016-0001-2, 74016-0001-3, 74016-0001-4, 74016-0001-5, 74016-0001-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
d655bb58-7960-5555-e053-2a95a90a6442a1b434ef-2eba-af73-e053-2a95a90ae22d2022-01-24WarningsExact identifier
spl set id: a1b434ef-2eba-af73-e053-2a95a90ae22d

Reported adverse events (FAERS/openFDA)#

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