Gentle Touch Antibacterial Hand Sanitizer

Manufacturer: Hill Chemical, Inc.
Effective date: 2021-05-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:45:06

Label at a glance#

ProductGentle Touch Antibacterial Hand Sanitizer

Active ingredientALCOHOL

Label structure6 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

• Put enough product in your palm to cover hands and rub hands together briskly until dry. • Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72.38%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

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

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

When using this product

OTC - WHEN USING SECTION

do not use it in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

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

• Put enough product in your palm to cover hands and rub hands together briskly until dry.

• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Purified Water USP.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Gentle Touch Antibacterial Hand Sanitizer
ALCOHOL
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78212-002	78212-002-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c200a13d-f90f-32e3-e053-2995a90aee11			a836a826-e5cd-1b1f-e053-2995a90a1379	2021-05-10	Warnings	Exact identifier spl id: c200a13d-f90f-32e3-e053-2995a90aee11 spl set id: a836a826-e5cd-1b1f-e053-2995a90a1379

Reported adverse events (FAERS/openFDA)#

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