FDA.reportPublic FDA data

FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM

Manufacturer
CWGC LA Inc.
Effective date
2023-09-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:04:12

Label at a glance#

ProductFRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

APPLY FOAM SANITIZER TO HANDS AND RUB OVER SURFACES OF BOTH HANDS FOR 15 SECONDS. NO RINSING REQUIRED.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

Use

INDICATIONS & USAGE SECTION

  • FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

WARNINGS

WARNINGS SECTION

For external use only.

WARNING: HARMFUL IF SWALLOWED.

CAUTION: KEEP OUT OF EYES. IN CASE OF ACCIDENTAL EYE CONTACT, FLUSH EYES THOROUGHLY WITH WATER. IF CONDITION WORSENS OR PERSISTS, CONTACT A PHYSICIAN. IF SWALLOWED, CONTACT A PHYSICIAN OR POISON CONTROL CENTER IMMEDIATELY.

When using this product

OTC - WHEN USING SECTION

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

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • APPLY FOAM SANITIZER TO HANDS AND RUB OVER SURFACES OF BOTH HANDS FOR 15 SECONDS. NO RINSING REQUIRED.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, COCO-GLUCOSIDE, LAURTRIMONIUM CHLORIDE, COCAMIDOPROPYLAMINE OXIDE, CITRIC ACID, FRAGRANCE.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Non-Alcohol Foam_Hand Sanitizer01b LBL_Non-Alcohol Foam_Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN5
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD5
1020365benzalkonium chloride 0.13 % Topical FoamSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70415-204-112025-01-30C16284748780-10191ceaa-673e-198a-e063-dbdaa90aec3eCWGC (as PLD) - Resource Solutions Fresh Hand Foaming Hand Sanitizer Non-Alcohol Foam (70415-204)
70415-204-112023-12-13C16284748780-10191ceaa-673e-198a-e063-dbdaa90aec3eCWGC (as PLD) - Resource Solutions Fresh Hand Foaming Hand Sanitizer Non-Alcohol Foam (70415-204)
70415-204-112023-07-28C16284748780-10191ceaa-673e-198a-e063-dbdaa90aec3eCWGC (as PLD) - Resource Solutions Fresh Hand Foaming Hand Sanitizer Non-Alcohol Foam (70415-204)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70415-204-11FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM1000 mL in 1 BOTTLESOLUTION10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70415-204FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM (BENZALKONIUM CHLORIDE) SOLUTION [CWGC LA INC.]5Legacy NDC, 1 package rows20231214_366b5115-5e66-4c94-8ff9-e0e6b2afbafe.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
70415-20470415-204-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO GLUCOSIDEICS790225BIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
05df821f-0926-180c-e063-6394a90ab4e0366b5115-5e66-4c94-8ff9-e0e6b2afbafe2023-09-21WarningsExact identifier
spl id: 05df821f-0926-180c-e063-6394a90ab4e0
spl set id: 366b5115-5e66-4c94-8ff9-e0e6b2afbafe

Reported adverse events (FAERS/openFDA)#

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