FDA.reportPublic FDA data

CareTouch Alcohol-Free Foaming Hand Sanitizer

Manufacturer
Future Diagnostics Llc
Effective date
2021-12-17
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:22:04

Label at a glance#

ProductCareTouch Alcohol-Free Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

• For hand washing to decrease bacteria on the skin.

Dosage and administration

• Apply small amount of foam to hands as desired, allow drying without wiping.

Storage and handling

• Store at room temperature • Avoid direct sunlight.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

• For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product if eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops and persist for more than 72 hours.

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

• Apply small amount of foam to hands as desired, allow drying without wiping.

Storage

STORAGE AND HANDLING SECTION

• Store at room temperature

• Avoid direct sunlight.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water, Betaine Anhydrous, Diazolidinyl urea, Phenoxyethanol, Palmitamidopropyltrimonium Chloride, Propylene Glycol, Sodium Citrate

SPL UNCLASSIFIED SECTION

Alcohol-Free Moisturizing Formula

Kills 99.99% of Germs*

Fragrance-Free & Hypoallergenic

Free of Triclosan, Parabens, Sulfates, Phthalates

*Kills 99.99% of common, harmful germs in just 15 seconds.

NDC 70393-456-25

ITEM# CTAFF10

NDC 70393-456-04

ITEM# CTAFF10-4

NDC 70393-456-01

ITEM# CTAFFS-T1

ITEM# FHS48

NDC# 70393-456-80

1800.758.3830

caretouchusa.com

Manufactured in China for Future Brands Brooklyn, NY 11220

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sanitize1sanitize1

image descriptionimage description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70393-456-80ML - Milliliter70393-456128fc85b-8517-4d50-8849-a37f509092f812021-09-07

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
70393-45670393-456-25, 70393-456-04, 70393-456-01, 70393-456-08, 70393-456-80

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
BETAINE3SCV180C9WIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
PALMITAMIDOPROPYLTRIMONIUM CHLORIDEN2U96D202FIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT

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
86742494-dd74-40f4-95c8-44c3371e66eac6989f81-889f-4451-ab44-9e6b6081898d2021-12-17WarningsExact identifier
spl id: 86742494-dd74-40f4-95c8-44c3371e66ea
spl set id: c6989f81-889f-4451-ab44-9e6b6081898d

Reported adverse events (FAERS/openFDA)#

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