D7 Foaming Hand Sanitizer

Manufacturer
Decon7 Systems, LLC
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:18:20

Label at a glance#

ProductD7 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

Pump a small amount of foam into palm of hand Rub thoroughly over surface of 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

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and conditions persist.

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

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over surface of hands
  • Rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Centrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

D7

D7 Foaming Hand Sanitizer

Foaming Non-Alcohol

Hand Sanitizer with

Benzalkonium Chloride by

Decon7 Systems

Kills up to 99.9999% of Germs

Cleans and Protects

Net Contents: 1 Gallon

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78245-20078245-200-01, 78245-200-02, 78245-200-03, 78245-200-05, 78245-200-04, 78245-200-06

Ingredients#

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

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

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
d3c0070a-7404-7d8c-e053-2a95a90a64c8a9ceae40-0ca9-12d0-e053-2a95a90adb782021-12-22WarningsExact identifier
spl set id: a9ceae40-0ca9-12d0-e053-2a95a90adb78

Reported adverse events (FAERS/openFDA)#

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