Non-Alcohol Foaming Hand Wash

Manufacturer
Arkansas Correctional Industries | Allison Corbitt
Effective date
2023-10-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:56:26

Label at a glance#

ProductNon-Alcohol Foaming Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

12BENZALKONIUM CHLORIDE 0.10%

1 See: INNERMOST LABEL.jpg

2 See: OUTERMOST LABEL.jpg

OTC - DO NOT USE SECTION

Do not use in the eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

OTC - PURPOSE SECTION

USE for waterless cleansing of hands to decrease soil on the skin

WARNINGS SECTION

WARNINGS

For external use only

Do not use in the eyes

Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS

Water, Laurtrimonium Chloride, Cetrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Fragrance.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

Place a palm full (approx. 5 grams) of product in one hand, spread on both hands, and rub into the skin until dry(approximately 1 to 2 minutes).
Place smaller amount (approx. 2.5 grams) into one hand, spread over both hands to wrist, and rub into the skin until dry(approximately 30 seconds).

INDICATIONS & USAGE SECTION

USE for waterless cleansing of hands to decrease soil on the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND WAS LABELHAND WAS LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN6
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD6
1038799benzalkonium chloride 0.1 % Topical FoamSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78890-001-012025-01-30C16284748780-12cef2736-a68e-d83d-e063-dadaa90ab31fNon-Alcohol Foaming Hand Sanitizing Wash
78890-001-022025-01-30C16284748780-12cef2736-a68e-d83d-e063-dadaa90ab31fNon-Alcohol Foaming Hand Sanitizing Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78890-001-01Non-Alcohol Foaming Hand Wash3785 mL in 1 JUGLIQUID37856
78890-001-02Non-Alcohol Foaming Hand Wash208198 mL in 1 DRUMLIQUID2081986

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78890-001NON-ALCOHOL FOAMING HAND WASH (BENZALKONIUM CHLORIDE 0.10%) LIQUID [ARKANSAS CORRECTIONAL INDUSTRIES]6Legacy NDC, 2 package rows20231005_a794a986-48fb-b7c0-e053-2a95a90a13cc.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78890-00178890-001-01, 78890-001-02

Ingredients#

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

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

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
06e944e8-71fd-9fe9-e063-6294a90a8c37a794a986-48fb-b7c0-e053-2a95a90a13cc2023-10-04WarningsExact identifier
spl id: 06e944e8-71fd-9fe9-e063-6294a90a8c37
spl set id: a794a986-48fb-b7c0-e053-2a95a90a13cc

Reported adverse events (FAERS/openFDA)#

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