Gentle Touch Antibacterial Hand

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

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

• For hand washing to decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

Pump a small amount of soap into palm of hand Rub thoroughly over all surfaces of both hands for 15 seconds Rinse with potable water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• For hand washing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops, or if condition persists for more than 72 hours.

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

Pump a small amount of soap into palm of hand
Rub thoroughly over all surfaces of both hands for 15 seconds
Rinse with potable water.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, sodium laurel ether sulfate, cocamide diethanolamine, cocoamidopropylbetaine, sodium chloride, citric acid, fragrance.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Soap

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Gentle Touch Antibacterial Hand
BENZALKONIUM CHLORIDE
WATER
SODIUM LAURETH-3 SULFATE
COCO DIETHANOLAMIDE
COCAMIDOPROPYL BETAINE
SODIUM CHLORIDE
CITRIC ACID MONOHYDRATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78212-000	78212-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM LAURETH-3 SULFATE	BPV390UAP0	IACT
COCO DIETHANOLAMIDE	92005F972D	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	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
c2007e3e-edaf-53f2-e053-2995a90aae08			a8365fc6-4282-a174-e053-2a95a90a5668	2021-05-10	Warnings	Exact identifier spl id: c2007e3e-edaf-53f2-e053-2995a90aae08 spl set id: a8365fc6-4282-a174-e053-2a95a90a5668

Reported adverse events (FAERS/openFDA)#

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