FDA.reportPublic FDA data

Foam Hand Sanitizer

Manufacturer
Rubbermaid Commercial Products LLC | NWL Netherlands Production B.V.
Effective date
2014-02-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:37:14

Label at a glance#

ProductFoam Hand Sanitizer
Active ingredientAlcohol
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

OTC - DO NOT USE SECTION

  • Flammable, keep away from fire or flame.
  • For external use only.
  • Do not ingest.
  • Avoid contact with eyes.

OTC - STOP USE SECTION

  • Discontinue use and consult a healthcare practitioner if irritation and redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), PEG-6 Caprilic/Capric Glycerides, Shea Butteramidopropyl Betaine, Disodium Lauriminodipropionate Tocopheryl Phosphates, Sodium Lactate, PEG/PPG-25/25 Dimethicone, Lactic Acid, PEG-14M

Questions?

OTC - QUESTIONS SECTION

1-800-347-9800 Mon–Fri, 8AM–5 PM EST

SPL UNCLASSIFIED SECTION

© 2010 Rubbermaid Commercial Products LLC
3124 Valley Avenue, Winchester, VA U.S.A. 22601-2694
www.rubbermaidcommercial.com

PRINCIPAL DISPLAY PANEL - 550 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rubbermaid®
Commercial Products

TC® ENRICHEDFOAM™

Alcohol Plus Hand Sanitizer
With Shea Butter & Vitamin E

550 mL (18.6 FL. OZ.)

Principal Display Panel - 550 mL Bottle Label
Principal Display Panel - 550 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65321-025-012023-10-27C16284748780-19855e2a2-32af-60a7-e053-dbdaa90a05bdTC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer
65321-025-022023-10-27C16284748780-19855e2a2-32af-60a7-e053-dbdaa90a05bdTC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer
65321-025-012019-11-27C16284748780-19855e2a2-32af-60a7-e053-dbdaa90a05bdTC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer
65321-025-022019-11-27C16284748780-19855e2a2-32af-60a7-e053-dbdaa90a05bdTC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M2
AlcoholACTIVE MOIETY3K9958V90M2
Lactic AcidINACTIVE INGREDIENT33X04XA5AT2
Sodium LactateINACTIVE INGREDIENTTU7HW0W0QT2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65321-02565321-025-03, 65321-025-01, 65321-025-04, 65321-025-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
Sodium LactateTU7HW0W0QTIACT
Lactic Acid33X04XA5ATIACT

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 · 25 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Sodium LactateSODIUM LACTATETU7HW0W0QTGEL / TOPICAL4 mgExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATSUPPOSITORY / VAGINALNAExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTSOLUTION / INTRAPERITONEAL0.45 %w/vExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATSOLUTION / TOPICAL7.22 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATINJECTION / INTRAVENOUS2232 mgExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATSUSPENSION / TOPICAL0.7 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATOINTMENT / TOPICALADJ PHExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTSOLUTION / TOPICAL0.93 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATSOLUTION / ORAL192 mgExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTSUSPENSION / ORAL20 mg/1mlExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATLOTION / TOPICAL5.7 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATAEROSOL, FOAM / TOPICAL11 mgExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATCREAM / VAGINAL0.81 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTINJECTION / INTRAVENOUS54 mgExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATINJECTION / INTRACARDIAC0.01 %w/vExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATTABLET / ORALADJ PHExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATINJECTION / INTRAMUSCULAR1.16 %w/vExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATINJECTION / SUBCUTANEOUS10 mgExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATCAPSULE / ORAL132 mgExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATCONCENTRATE / ORAL50 mg/5mlExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS18.7 mgExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATINJECTION, SOLUTION / INTRAVENOUS87 mgExact identifier — unii candidate
18 equally ranked IID candidates
Sodium LactateSODIUM LACTATETU7HW0W0QTINJECTION, SOLUTION / INFILTRATION0.17 %v/vExact identifier — unii candidate
7 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATGEL / TOPICAL30 mgExact identifier — unii candidate
18 equally ranked IID candidates
Lactic AcidLACTIC ACID33X04XA5ATCREAM / TOPICAL1 %w/wExact identifier — unii candidate
18 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
f4b164db-cb41-4da7-9607-6fa4931b362164086ae6-3909-4f72-99ed-9f1699ec28712014-02-20WarningsExact identifier
spl set id: 64086ae6-3909-4f72-99ed-9f1699ec2871

Reported adverse events (FAERS/openFDA)#

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