FDA.reportPublic FDA data

InstantFOAM alcohol hand sanitizer

Manufacturer
Deb USA, Inc. | Deb Worldwide Healthcare Inc.
Effective date
2010-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:35

Label at a glance#

ProductInstantFOAM alcohol hand sanitizer
Active ingredientAlcohol
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                                          

Ethyl Alcohol 72%

OTC - PURPOSE SECTION


Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to reduce bacteria on skin


WARNINGS SECTION

Warnings

For external use only

Avoid contact with eyes

Flammable

Keep away from flame or fire

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Consult physician or poison control if ingested.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply one shot to dry hands

Rub into skin

No rinsing required

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, n-Propanol, Cocoglucoside, Glyceryl Oleate, PEG-7 Glyceryl Cocoate, PEG-200 Hydrogenated Glyceryl Palmate, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Behentrimonium Chloride, Bis-PEG-12 Dimethicone


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

deb

Instant Foam

alcohol hand sanitizer

refreshing

no water required

use anywhere, any time

use everyday

Kills>99.9999%

of common germs in 15 seconds

Made in Canada

Worldwide Patent Pending

deb foam technology

NSF

Nonfood Compounds Program Listed E-3 140062

01827-01-116

1 Liter - 33.8 Fluid Ounces

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1085908ethanol 72 % Topical FoamPSN1
1085908ethanol 0.72 ML/ML Topical FoamSCD1
1085908ethanol 72 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11084-017-012019-10-21C16284748780-1956f9ecf-d218-621f-e053-dbdaa90a74adDrug Facts
11084-017-272019-10-21C16284748780-1956f9ecf-d218-621f-e053-dbdaa90a74adDrug Facts
11084-017-402019-10-21C16284748780-1956f9ecf-d218-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11084-017-01InstantFOAM alcohol hand sanitizer47 mL in 1 BOTTLE, PUMPLIQUID471
11084-017-27InstantFOAM alcohol hand sanitizer1000 mL in 1 BOTTLE, SPRAYLIQUID10001
11084-017-40InstantFOAM alcohol hand sanitizer400 mL in 1 BOTTLE, SPRAYLIQUID4001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11084-017INSTANTFOAM ALCOHOL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [DEB USA, INC.]1Legacy NDC, 3 package rows20100823_929eb8b6-0b39-4800-97b9-fc2fc910ccc7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M1
AlcoholACTIVE MOIETY3K9958V90M1
Behentrimonium ChlorideINACTIVE INGREDIENTX7GNG3S47T1
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH11
Propyl AlcoholINACTIVE INGREDIENT96F264O9SV1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11084-01711084-017-01, 11084-017-40, 11084-017-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
Propyl Alcohol96F264O9SVIACT
Behentrimonium ChlorideX7GNG3S47TIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Propyl AlcoholPROPYL ALCOHOL96F264O9SVSOLUTION / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
Propyl AlcoholPROPYL ALCOHOL96F264O9SVOINTMENT / TOPICAL10 %w/wExact identifier — unii candidate
3 equally ranked IID candidates
Propyl AlcoholPROPYL ALCOHOL96F264O9SVPOWDER / TOPICAL0.4 mg/mgExact identifier — unii candidate
3 equally ranked IID candidates

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
7c1bda11-b9c7-4aa1-ad2f-3a101bcdced6929eb8b6-0b39-4800-97b9-fc2fc910ccc72010-08-19WarningsExact identifier
spl id: 7c1bda11-b9c7-4aa1-ad2f-3a101bcdced6
spl set id: 929eb8b6-0b39-4800-97b9-fc2fc910ccc7

Reported adverse events (FAERS/openFDA)#

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