MARKET AMERICA ANTIBACTERIAL HAND SANITIZER- benzalkonium chloride spray

Market America Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Market America Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cemi International, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

INDICATIONS & USAGE

Use For hand sanitizing to decrease bacteria on the skin.

Warnings

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.

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

STORAGE AND HANDLING

Other Information May discolor certain fabrics or surfaces

DOSAGE & ADMINISTRATION

Directions 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 INGREDIENT

Inactive ingredients 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

INGREDIENTS AND APPEARANCE

MARKET AMERICA ANTIBACTERIAL HAND SANITIZER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73741-106
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
UREA (UNII: 8W8T17847W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73741-106-04	88.7 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/14/2020

Labeler - Cemi International, Inc (015038336)

Establishment
Name	Address	ID/FEI	Business Operations
Cemi International, Inc		015038336	manufacture(73741-106)