FDA.reportPublic FDA data

Personal CARE

Manufacturer
Delta Brands & Products LLC
Effective date
2018-04-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:59:59

Label at a glance#

ProductPersonal CARE FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

for washing hands to decrease bacteria on the skin

Dosage and administration

■ pump into hands ■ lather vigorously for at least 15 seconds ■ rinse and dry thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for washing hands to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or rash develops

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

■ pump into hands ■ lather vigorously for at least 15 seconds ■ rinse and dry thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), laureth-9, disodium cocoamphodiacetate, polyquaternium-10, citric acid, fragrance, glycerin, methylchloroisothiazolinone, methylisothiazolinone, FD&C blue no. 1, FD&C yellow no. 5

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Paackage LabelPaackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72133-150-752020-09-27C16284748780-1ab0e2407-29eb-f274-e053-dbdaa90a6471Drug Facts
72133-150-752020-09-25C16284748780-1ab0e2407-29eb-f274-e053-dbdaa90a6471Drug Facts
72133-150-752020-07-22C16284748780-1ab0e2407-29eb-f274-e053-dbdaa90a6471Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72133-150PERSONAL CARE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DELTA BRANDS & PRODUCTS LLC]1Legacy NDC20180413_69adf628-0308-8437-e053-2991aa0abc9a.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72133-15072133-150-75

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
EDETATE SODIUM TETRAHYDRATEL13NHD21X6IACT
WATER059QF0KO0RIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
POLIDOCANOL0AWH8BFG9AIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
69adf628-030a-8437-e053-2991aa0abc9a69adf628-0308-8437-e053-2991aa0abc9a2018-04-12WarningsExact identifier
spl id: 69adf628-030a-8437-e053-2991aa0abc9a
spl set id: 69adf628-0308-8437-e053-2991aa0abc9a

Reported adverse events (FAERS/openFDA)#

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