FDA.reportPublic FDA data

Market America Antibacterial Hand Sanitizer

Manufacturer
Market America, Inc. | Cemi International, Inc
Effective date
2021-03-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:49

Label at a glance#

ProductMarket America Antibacterial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

• wet hands thoroughly with product and rub hands together until dry. • children under 6 years of age should be supervised when using this product • Not recommended for infants

Storage and handling

• May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product avoid contact with eyes. In case of contact with eyes, flush eyes with water.

Stop use and ask a doctor if irritation or rash develops and lasts.

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.

Other Information

STORAGE AND HANDLING SECTION

• May discolor certain fabrics or surfaces

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and rub hands together until dry. • children under 6 years of age should be supervised when using this product • Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ionized water, Urea

SPL UNCLASSIFIED SECTION

CONVERT SPENDING INTO EARNING

alcohol-free

triclosan-free &

fragrance free

Eliminates 99.99% of Germs

SHOPPING ANNUITY® BRAND

BAC-D

BACTERIAL DEFENSE

Manufactured for Market America, Inc.,
1302 Pleasant Ridge Rd., Greensboro, NC 27409

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN1
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD1
1039012benzalkonium chloride 0.13 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76209-117-032023-01-30C16284748780-1f386c64a-1b88-0266-e053-dadaa90a7c1aANTIBACTERIAL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76209-117-03Market America Antibacterial Hand Sanitizer88.7 mL in 1 BOTTLE, SPRAYSPRAY88.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76209-117MARKET AMERICA ANTIBACTERIAL HAND SANITIZER (BENZALKONIUM CHLORIDE) SPRAY [MARKET AMERICA, INC.]1Legacy NDC, 1 package rows20210421_a182fd1f-cae8-4a07-bf70-234b283495b2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76209-11776209-117-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
UREA8W8T17847WIACT

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
96875037-bd47-4060-9034-99aebadaa9eda182fd1f-cae8-4a07-bf70-234b283495b22021-03-15WarningsExact identifier
spl id: 96875037-bd47-4060-9034-99aebadaa9ed
spl set id: a182fd1f-cae8-4a07-bf70-234b283495b2

Reported adverse events (FAERS/openFDA)#

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