BENZALKONIUM CHLORIDE liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Available from:

S. P. Richards Company

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antibacterial for handwashing to decrease bacteria on the skin - irritation or redness develops - condition persists for more than 72 hours

Authorization status:

OTC monograph not final

Summary of Product characteristics

BENZALKONIUM CHLORIDE- BENZALKONIUM CHLORIDE LIQUID
S. P. RICHARDS COMPANY
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may_
_be marketed if they comply with applicable regulations and policies.
FDA has not_
_evaluated whether this product complies._
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GENUINE JOE ANTIBACTERIAL FOAMING HAND WASH 628.002/628AD/AE
ACTIVE INGREDIENT
Benzalkonium chloride 0.13%
PURPOSE
Antibacterial
USE
for handwashing to decrease bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY: HANDS ONLY
WHEN USING THIS PRODUCT
avoid contact with eyes. If contact occurs, rinse eyes thoroughly with
water.
STOP USE AND ASK A DOCTOR IF
irritation or redness develops
condition persists for more than 72 hours
KEEP OUT OF REACH OF CHILDREN.
if swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
apply palmful to dry hands
scrub thoroughly
rinse thoroughly
INACTIVE INGREDIENTS
water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine
oxide,
water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine
oxide,
myristamidopropylamine oxide, glycerin, fragrance, citric acid,
tetrasodium EDTA,
benzophenone-4, sodium benzoate, blue 1, red 33
ADVERSE REACTION
Distributed by
S.P. Rochards Company, Smyrna, GA 30082
www.genuinejoe.com
PRINCIPAL DISPLAY PANEL
GENUINE JOE
FOAMING HAND SOAP
Antibacterial
7.5 FL OZ (221 mL)
BENZALKONIUM CHLORIDE
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:62832-628
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1.3 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8Q