GP PBU ANTIMICROBIAL FOAM- benzalkonium chloride solution

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

Werkstoffen:

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

Beschikbaar vanaf:

Georgia Pacific Consumer Products

Toedieningsweg:

TOPICAL

Prescription-type:

OTC DRUG

therapeutische indicaties:

Antiseptic Handwash to help reduce bacteria that potentially can cause disease.

Autorisatie-status:

OTC monograph not final

Productkenmerken

GP PBU ANTIMICROBIAL FOAM- BENZALKONIUM CHLORIDE SOLUTION
GEORGIA PACIFIC CONSUMER PRODUCTS
_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._
----------
54622-313
_DRUG FACTS_
_ACTIVE INGREDIENT_
Benzalkonium chloride, 0.13%
_PURPOSE_
Antiseptic
_USE_
Handwash to help reduce bacteria that potentially can cause disease.
_WARNINGS_
For external use only
WHEN USING THIS PRODUCT
Avoid contact with the eyes. In case of eye contact, flush with water.
STOP USE
if irritation or redness developes. If condition persists for more
than 72 hours consult a
doctor.
KEEP OUT OF REACH OF CHILDREN
If swallowed, seek immediate medical attention or call a poison
control center.
_DIRECTIONS_
Wet hands, apply soap, rub hands togetehr vigorously for at least 20
seconds.
Rinse and dry hands thoroughly.
_INACTIVE INGREDIENTS_
Water (Aqua), Lauramine Oxide, Lauryl Betaine, Glycerin, Laurtrimonium
Chloride,
Sodium PCA, Tocopheryl Acetate, Oleth-10, Tetrasodium EDTA, Citric
Acid, Red 40,
Yellow 6, Fragrance
GP PBU ANTIMICROBIAL FOAM
benzalkonium chloride solution
Georgia Pacific Consumer Products
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:54622-313
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
0.13 g
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
LAURYL BETAINE (UNII: Y4P927Q133)
GLYCERIN (UNII: PDC6A3C0OX)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C RED NO. 40 (UNII: WZB9127XOA)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
OLETH-10 (UNII: JD797EF70J)
PACKAGING
# ITEM CO