FDA.reportPublic FDA data

Deb InstantFOAM Non-Alcohol PURE

Manufacturer
SC Johnson Professional USA, Inc. | SC Johnson Professional CA Inc.
Effective date
2022-12-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:43:07

Label at a glance#

ProductDeb InstantFOAM Non-Alcohol PURE
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

for hand sanitizing to reduce bacteria on the skin

Dosage and administration

apply one shot to dry hands, rub into skin no rinsing required

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE, 0.13%   

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for hand sanitizing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

INSTRUCTIONS FOR USE SECTION

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush with water.

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

apply one shot to dry hands, rub into skin

no rinsing required

Inactive ingredients

INACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF JUICE, AQUA (WATER), COCAMIDOPROPYL BETAINE, LAURAMINE OXIDE, MAGNESIUM CHLORIDE, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, TETRASODIUM EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

deb stoko

Deb InstantFOAM(R) Non-Alcohol PURE

Dye & Fragrance Free Hand Sanitizer

Antiseptico para manos en espuma - sin alcohol, sin colorante y sin perfume

SANITIZE

NON-ALCOHOL

DCN8901/1116

Deb USA, Inc. Charlotte,

NC 28217. 1-800-248-7190

www.debgroup.com

Made in USA

1 L

(33.8 fl oz)

55857-DCN8901 InstantFOAM NonAlcohol PURE-1L-V9.jpg55857-DCN8901 InstantFOAM NonAlcohol PURE-1L-V9.jpg

55857-DCN8901 InstantFOAM NonAlcohol PURE-1L-V9.jpg55857-DCN8901 InstantFOAM NonAlcohol PURE-1L-V9.jpg

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-00111084-001-01, 11084-001-40, 11084-001-27, 11084-001-12, 11084-001-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
MAGNESIUM NITRATE77CBG3UN78IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE SODIUMMP1J8420LUIACT

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
e88a3489-a6d4-4047-954f-251581b0a5d06b03bc9d-3f3e-4b59-bef8-d68335233a9c2022-12-22WarningsExact identifier
spl id: e88a3489-a6d4-4047-954f-251581b0a5d0
spl set id: 6b03bc9d-3f3e-4b59-bef8-d68335233a9c

Reported adverse events (FAERS/openFDA)#

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