FDA.reportPublic FDA data

ProFormance Series Foam Alcohol Hand Sanitizer

Manufacturer
Pro-Link, Inc. | Deb USA, Inc. | Deb Worldwide Healthcare Inc.
Effective date
2011-01-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:26:56

Label at a glance#

ProductProFormance Series Foam 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

Flammable: Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.

In case of eye contact, flush with water.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply one shot of foaming sanitizer to dry hands

Rub into skin

No rinsing required

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ProFormance Series

Foam Alcohol Sanitizer

Pro-Link Green

Certified EcoLogo

Certified Instant Hand Antiseptic CCD-170

MSA1000

Distributed exclusively by:

Pro-Link, Inc.

1 Liter

33.8 Fluid Ounces

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1085908ethanol 72 % Topical FoamPSN3
1085908ethanol 0.72 ML/ML Topical FoamSCD3
1085908ethanol 72 % Topical FoamSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66908-107-122019-10-29C16284748780-1960f7f55-cf1d-8e05-e053-dbdaa90a074aDrug Facts
66908-107-272019-10-29C16284748780-1960f7f55-cf1d-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66908-107-12ProFormance Series Foam Alcohol Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10003
66908-107-27ProFormance Series Foam Alcohol Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66908-107PROFORMANCE SERIES FOAM ALCOHOL HAND SANITIZER (ETHYL ALCOHOL ) LIQUID [PRO-LINK, INC.]3Legacy NDC, 2 package rows20110118_47361568-2f2f-407c-967e-7c080b7f8a4a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M3
ALCOHOLACTIVE MOIETY3K9958V90M3
BEHENTRIMONIUM CHLORIDEINACTIVE INGREDIENTX7GNG3S47T3
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH13
PROPYL ALCOHOLINACTIVE INGREDIENT96F264O9SV3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
66908-10766908-107-27, 66908-107-12

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 ALCOHOL96F264O9SVPOWDER / TOPICAL0.4 mg/mgExact identifier — unii candidate
3 equally ranked IID candidates
PROPYL ALCOHOLPROPYL ALCOHOL96F264O9SVOINTMENT / TOPICAL10 %w/wExact identifier — unii candidate
3 equally ranked IID candidates
PROPYL ALCOHOLPROPYL ALCOHOL96F264O9SVSOLUTION / TOPICALNAExact 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
987b5df0-f88f-4d4b-af0b-19322ee9061847361568-2f2f-407c-967e-7c080b7f8a4a2011-01-17WarningsExact identifier
spl id: 987b5df0-f88f-4d4b-af0b-19322ee90618
spl set id: 47361568-2f2f-407c-967e-7c080b7f8a4a

Reported adverse events (FAERS/openFDA)#

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