ENMOTION ANTIMICROBIAL FOAM WITH MOISTURIZERS TRANQUIL ALOE- benzalkonium chloride solution

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

Wirkstoff:

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

Verfügbar ab:

Georgia-Pacific Consumer Products

Verabreichungsweg:

TOPICAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

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

Berechtigungsstatus:

OTC monograph not final

Fachinformation

ENMOTION ANTIMICROBIAL FOAM WITH MOISTURIZERS TRANQUIL ALOE-
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._
----------
54622-315
_DRUG FACTS_
_ACTIVE INGREDIENT_
Benzalkonium chloride, 0.13% w/w
_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 eyes. In case of eye contact, flush with water.
STOP USE
if irritation or redness develops. 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 together vigorously for at least 20
seconds.
Rinse and dry hands thoroughly with a disposable paper towel.
_INACTIVE INGREDIENTS_
Water (Aqua),Lauramine Oxide, Lauryl Betaine, Laurtrimonium
Chloride, Glycerin, Sodium PCA, Tocopheryl Acetate,
Oleth-10, Aloe Barbadensis Leaf Juice, Chamomilla
Recutita (Matricaria) Extract, Camellia Sinensis Leaf
Extract, Avena Sativa (Oat) Kernel Extract, Euterpe
Oleracea Fruit Extract, Tetrasodium EDTA, Citric
Acid, Fragrance, FD&C Green #5, FD&C Yellow #10
ENMOTION ANTIMICROBIAL FOAM WITH MOISTURIZERS TRANQUIL
ALOE
benzalkonium chloride solution
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:54622-315
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
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
LAURYL BETAINE (UNII: Y4P927Q133)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
SODIUM PIDOLATE (UNII: 1V74VH163T)
OLETH-10 (UNII: JD797EF70J)
ALO