First Street Antibacterial Liquid Hand

Manufacturer
Amerifoods Trading Company | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:42:44

Label at a glance#

ProductFirst Street Antibacterial Liquid Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin.

Dosage and administration

-Apply small amount of product to wet hands -Work into lather and rinse thoroughly -Dry hands

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride........0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing 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

or if condition persists.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

or contact Posion Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

-Apply small amount of product to wet hands

-Work into lather and rinse thoroughly

-Dry hands

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Caprylyl/Capryl Glucoside, Citric Acid, Cocamide MIPA, Cocamidopropyl Betaine, Fragrance, Glycerin, Lauryl Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchloroisothiazolinone, Methylisothiazolinone, PEG 150 Distearate, FD&C Red #40, Tetrasodium EDTA, Water, FD&C Yellow #5

First Street Antibacterial 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 SoapPSN3
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD3
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY3
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61504-551-01First Street Antibacterial Liquid Hand3.80564 kg in 1 BOTTLE, PLASTICLIQUID3.805643
61504-551-02First Street Antibacterial Liquid Hand1 in 1 BOXLIQUID13
61504-551-16First Street Antibacterial Liquid Hand.0568 kg in 1 BOTTLE, PLASTICLIQUID.05683
61504-551-17First Street Antibacterial Liquid Hand1 in 1 BOXLIQUID13
61504-551-64First Street Antibacterial Liquid Hand1.91 kg in 1 BOTTLE, PLASTICLIQUID1.913

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
61504-55161504-551-01, 61504-551-02, 61504-551-16, 61504-551-17, 61504-551-64

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
22024-12-13full-release2026-06-01 00:43:39

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
First Street Antibacterial Liquid HandBENZALKONIUM CHLORIDEAmerifoods Trading Companye9d5fefa-970b-42ba-8139-18e5644153442025-11-06WarningsExact identifier
ndc (package): 61504-551-64
ndc (package): 61504-551-17
ndc (package): 61504-551-02
ndc (package): 61504-551-16
ndc (package): 61504-551-01
ndc (product): 61504-551
ndc11 (package): 61504055116
ndc11 (package): 61504055102
ndc11 (package): 61504055164
ndc11 (package): 61504055117
ndc11 (package): 61504055101
spl id: d4170919-ca2d-4555-84b5-1b3773324699
spl set id: e9d5fefa-970b-42ba-8139-18e564415344

Reported adverse events (FAERS/openFDA)#

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