FOAMING HAND- benzalkonium chloride lotion

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Aktīvā sastāvdaļa:

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

Pieejams no:

Vi-Jon, LLC

Ievadīšanas:

TOPICAL

Receptes veids:

OTC DRUG

Ārstēšanas norādes:

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

Autorizācija statuss:

OTC monograph not final

Produkta apraksts

FOAMING HAND- BENZALKONIUM CHLORIDE LOTION
VI-JON, LLC
_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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ANTIBACTERIAL FOAMING HAND SOAP
224.000/224AA
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 with water.
STOP USE AND ASK A DOCTOR IF
irritation or redness develop
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_
wet hands
apply palmful to hands
scrub thoroughly
rinse thoroughly
_INACTIVE INGREDIENTS_
water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine
oxide,
myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA,
sodium benzoate
ADVERSE EVENT
Manufactured By: Vi-Jon, Inc.
St. Louis, Mo 63114
PRINCIPAL DISPLAY PANEL
germ-X
Professional
ANTIBACTERIAL
FOAMING
HAND SOAP
1000 ML (33.8 FL OZ)
FOAMING HAND
benzalkonium chloride lotion
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:11344-224
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
BENZ ALKONIUM
1.3 mg
UNII:7N6JUD5X6Y)
CHLORIDE
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: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:11344-
224-08
3785 mL