Pioneer Eclipse Touche Foaming Non-Alcohol Hand Sanitizer

Manufacturer
CWGC LA Inc.
Effective date
2023-09-21
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:56:15

Label at a glance#

ProductPioneer Eclipse Touche Foaming Non-Alcohol Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Apply foam sanitizer to hands. 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

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

Avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and persists.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply foam sanitizer to hands.
  • 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

Pioneer_Non-Alcohol Hand Sanitizer_ChinaPioneer_Non-Alcohol Hand Sanitizer_China

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN8
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD8
1020365benzalkonium chloride 0.13 % Topical FoamSY8

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
70415-305-012025-01-30C16284748780-12cef2736-9076-d83d-e063-dadaa90ab31fCWGC - Pioneer Eclipse Touché Foaming Non-Alcohol Hand Sanitizer (70415-305)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70415-305-01Pioneer Eclipse Touche Foaming Non-Alcohol Hand Sanitizer1000 mL in 1 BOTTLESOLUTION10008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70415-305PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [CWGC LA INC.]8Legacy NDC, 1 package rows20230922_1cecdac5-dcd3-424c-b747-f7769a4a4f95.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
70415-30570415-305-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
05df5eea-c8ac-7d7a-e063-6294a90a68ac1cecdac5-dcd3-424c-b747-f7769a4a4f952023-09-21WarningsExact identifier
spl id: 05df5eea-c8ac-7d7a-e063-6294a90a68ac
spl set id: 1cecdac5-dcd3-424c-b747-f7769a4a4f95

Reported adverse events (FAERS/openFDA)#

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