FDA.reportPublic FDA data

Members Mark

Manufacturer
Ecolab Inc.
Effective date
2024-08-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:16:31

Label at a glance#

ProductMembers Mark
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

wet hands and apply foam scrub hands and forearms rinse thoroughly and dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin

Warning

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in eyes

When using the product

OTC - WHEN USING SECTION

  • if in eyes, rinse promptly and thoroughly with water
  • discontinue use if irritation and redness develop

Stop use and ask a physician if

OTC - ASK DOCTOR SECTION

  • Skin irritation or redness occurs for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and apply foam
  • scrub hands and forearms
  • rinse thoroughly and dry

Other information

REFERENCES SECTION

  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information, call 866.897.8061

INACTIVE INGREDIENT SECTION

Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, myristamine oxide, phenoxyethanol, polyquaternium 7, citric acid, myristamide DIPA, methyl gluceth-20, glyceryl caprylate/caprate, PEG-12 dimethicone, potassium citrate, fragrance, FD&C blue 1

OTC - QUESTIONS SECTION

Questions? call 866.999.7484

Representative Label and Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Member's Mark

COMMERCIAL

FOAMING

ANTIBACTERIAL

HAND SOAP

Available at Sam's Club and samsclub.com

Net 33.8 fl. oz. (1000 ml)

766173-00 766173/5002/0820

ECOLAB • 4050 Corporate Drive STE 100

Grapevine, TX 76051

© 2020 Ecolab • Ecolab USA Inc., All rights reserved.

Representative labelRepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSN5
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCD5
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSY5

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-572-12Members Mark1000 mL in 1 BAGSOLUTION10005
47593-572-26Members Mark1000 mL in 1 BAGSOLUTION10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47593-572MEMBERS MARK (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.]5Current NDC, Legacy NDC, 2 package rows20240805_40342279-c73d-4644-8569-2b44982149e2.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-57247593-572-12, 47593-572-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C BLUE NO. 1H3R47K3TBDIACT
POTASSIUM CITRATEEE90ONI6FFIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
GLYCERYL MONO- AND DICAPRYLOCAPRATEU72Q2I8C85IACT
METHYL GLUCETH-20J3QD0LD11PIACT
MYRISTIC DIISOPROPANOLAMIDE17DN142CTKIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MYRISTAMINE OXIDEJ086PM3RRTIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
GLYCERINPDC6A3C0OXIACT
POLYETHYLENE GLYCOL 8000Q662QK8M3BIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
WATER059QF0KO0RIACT
COCAMINE OXIDEQWA2IZI6FIIACT

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
Members MarkBENZALKONIUM CHLORIDEEcolab Inc.40342279-c73d-4644-8569-2b44982149e22024-08-02WarningsExact identifier
ndc (package): 47593-572-12
ndc (package): 47593-572-26
ndc (product): 47593-572
ndc11 (package): 47593057212
ndc11 (package): 47593057226
spl id: b94c8057-361a-4044-96f6-98e57772f958
spl set id: 40342279-c73d-4644-8569-2b44982149e2

Reported adverse events (FAERS/openFDA)#

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