FDA.reportPublic FDA data

Decon7 Antiseptic Foaming Hand Sanitizer

Manufacturer
Decon7 Systems, LLC
Effective date
2022-10-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:07

Label at a glance#

ProductDecon7 Antiseptic Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 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

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 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Decon7 Antiseptic Foaming Hand Sanitizer
Manufactured in the USA for: D7™ DECON SEVEN

110 North Freeport Parkway, Suite 120, Coppell, TX 75019

844-727-FOAM / info@decon7.com

1.7 fl oz (50 mL)

24/7 Emergency Response,

Contact Chemtrec 800-424-9300

50 mL label50 mL label

1000 mL label1000 mL label

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78245-10178245-101-01, 78245-101-03, 78245-101-05, 78245-101-04, 78245-101-06

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
NameUNIIKind
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
ACETAMIDOETHOXYETHANOLLVX2APC4XRIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
eb665069-0d05-c524-e053-2a95a90aeab2d344f694-0055-d2d1-e053-2995a90a8f822022-10-19WarningsExact identifier
spl id: eb665069-0d05-c524-e053-2a95a90aeab2
spl set id: d344f694-0055-d2d1-e053-2995a90a8f82

Reported adverse events (FAERS/openFDA)#

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