Metro Antimicrobial Lotion Hand Soap

Manufacturer
Maintex | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:42:41

Label at a glance#

ProductMetro Antimicrobial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

-Apply to wet hands. -Work into a lather and  rinse thoroughly. -Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride .13

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When Using this Product

GENERAL PRECAUTIONS SECTION

Avoid contact with the eyes.

In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops

and conditions persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

or contact a Posion Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

-Apply to wet hands.

-Work into a lather and  rinse thoroughly.

-Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Caprylyl/Capryl Glucoside, Citric Acid, Cocamidopropyl Betaine, Fragrance, Glycerin, Laurel Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchoroisothiazolinone, Methylisothiazolinone FD&C Red #40, Tetrasodium EDTA, Water, FD&C Yellow #5

Metro Antimicrobial Lotion Hand Soap

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130765294116812GTIN-13: 0765294116812
EAN-13: 0765294116812
GTIN-12: 765294116812
UPC-A: 765294116812
GTIN storage (14 digits): 00765294116812
2900-116807MTA revised inactive ingredients 1-9-25.jpg
QR code linkQR Codemetrobarcode.azurewebsites.net/Home/GetFile?id=924ff7c2-1b10-45cf-8936-a973793c3aee2900-116807MTA revised inactive ingredients 1-9-25.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77617-023-01Metro Antimicrobial Hand3.8057 kg in 1 BOTTLE, PLASTICLIQUID3.80572
77617-023-02Metro Antimicrobial Hand1 in 1 BOXLIQUID12

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
77617-02377617-023-01, 77617-023-02

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-01-21full-release2026-06-01 00:53:20

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
Metro Antimicrobial HandBENZALKONIUM CHLORIDEMaintexa84d83dd-2445-4d0f-b763-2c69e8248cf92025-11-06WarningsExact identifier
ndc (package): 77617-023-02
ndc (package): 77617-023-01
ndc (product): 77617-023
ndc11 (package): 77617002301
ndc11 (package): 77617002302
spl id: 500a1f5e-1050-42f0-9d9a-a8c61b9330b8
spl set id: a84d83dd-2445-4d0f-b763-2c69e8248cf9

Reported adverse events (FAERS/openFDA)#

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