D7 Foaming Hand Sanitizer

Manufacturer: Decon7 Systems, LLC
Effective date: 2021-01-01
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:57:51

Label at a glance#

ProductD7 Foaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

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

Dosage and administration

Apply small amount of foam into palm of hand Rub hands together briskly covering surface of hands until dry

Contacts and useful links#

PhoneLabel contact800-424-9300

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

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of eye contact, flush eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last 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 into palm of hand
Rub hands together briskly covering surface of hands until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

Decon7 Antiseptic

Foaming Hand Sanitizer

Manufactured in the USA for: D7 / Decon Seven

8541 E Anderson Drive, Suite 106

Scottsdale, AZ 85255

844-727-FOAM

info@decon7.com

24/7 Emergency Response,

Contact Chemtrec 800-424-9300

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

label 2

label 3

Products#

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

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

D7 Foaming Hand Sanitizer
Benzalkonium Chloride
DIHYDROXYETHYL COCAMINE OXIDE
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
CITRIC ACID MONOHYDRATE
WATER
ACETAMIDOETHOXYETHANOL
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78245-100	78245-100-01, 78245-100-02, 78245-100-03, 78245-100-04, 78245-100-05, 78245-100-07

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
DIHYDROXYETHYL COCAMINE OXIDE	8AR51R3BL5	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
ACETAMIDOETHOXYETHANOL	LVX2APC4XR	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
d3bff562-f38c-58a5-e053-2a95a90a56d5			a9cc027b-295e-4b36-e053-2a95a90a45ce	2021-12-22	Warnings	Exact identifier spl set id: a9cc027b-295e-4b36-e053-2a95a90a45ce

Reported adverse events (FAERS/openFDA)#

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