Gentle Touch Foaming 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 Foaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

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

Dosage and administration

• Pump a small amount of foam into palm of hand • Rub thoroughly over all surfaces of both hands • Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• For hand sanitizing 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 redness 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 foam into palm of hand

• Rub thoroughly over all surfaces of both hands

• Rub hands together briskly until dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid, fragrance

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Products#

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

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

Gentle Touch Foaming Hand Sanitizer
BENZALKONIUM CHLORIDE
WATER
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE
DIHYDROXYETHYL COCAMINE OXIDE
ACETAMIDOETHOXYETHANOL
CITRIC ACID MONOHYDRATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78212-001	78212-001-01

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT
DIHYDROXYETHYL COCAMINE OXIDE	8AR51R3BL5	IACT
ACETAMIDOETHOXYETHANOL	LVX2APC4XR	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
c200a13d-f912-32e3-e053-2995a90aee11			a8369e41-63d4-63fd-e053-2995a90affad	2021-05-10	Warnings	Exact identifier spl id: c200a13d-f912-32e3-e053-2995a90aee11 spl set id: a8369e41-63d4-63fd-e053-2995a90affad

Reported adverse events (FAERS/openFDA)#

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