FDA.reportPublic FDA data

FOAMING HAND SANITIZER

Manufacturer
SAFEWAY INC
Effective date
2010-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:13

Label at a glance#

ProductFOAMING HAND SANITIZER WITH ALOE
Active ingredientBENZALKONIUM CHLORIDE
Label structure5 sections

Indications and uses

USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE. DIRECTIONS: PUMP ENOUGH PRODUCT TO YOUR PALM TO THOROUGHLY COVER YOUR HANDS, RUB TOGETHER UNTIL DRY.

Dosage and administration

USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE. DIRECTIONS: PUMP ENOUGH PRODUCT TO YOUR PALM TO THOROUGHLY COVER YOUR HANDS, RUB TOGETHER UNTIL DRY.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE  0.1% (ANTISEPTIC)

USES AND DIRECTIONS

OTC - PURPOSE SECTION

  • USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
  • DIRECTIONS: PUMP ENOUGH PRODUCT TO YOUR PALM TO THOROUGHLY COVER YOUR HANDS, RUB TOGETHER UNTIL DRY.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES WITH WATER.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

  • SKIN IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

PACKAGE FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

  • 8OZ FRONT AND BACK LABELS: safeway8.jpg8OZ FRONT AND BACK LABELS8OZ FRONT AND BACK LABELS

QUESTIONS/COMMENTS?

OTC - QUESTIONS SECTION

1-888-723-3929

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21130-240-082020-01-31C16284748780-19d75b9d0-afba-f424-e053-dadaa90a57ceDRUG FACTS BOX (BACK LABEL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-240-08FOAMING HAND SANITIZERWITH ALOE236 mL in 1 BOTTLE, PUMPLIQUID2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-240FOAMING HAND SANITIZER WITH ALOE (BENZALKONIUM CHLORIDE) LIQUID [SAFEWAY INC]1Legacy NDC, 1 package rows20100715_3193225a-ef66-49e7-93f8-e14afaf2dd0e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21130-24021130-240-08

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
a213c774-4879-46ec-8ebc-c6e7283df1393193225a-ef66-49e7-93f8-e14afaf2dd0e2010-07-14WarningsExact identifier
spl id: a213c774-4879-46ec-8ebc-c6e7283df139
spl set id: 3193225a-ef66-49e7-93f8-e14afaf2dd0e

Reported adverse events (FAERS/openFDA)#

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