ANTIBACTERIAL- benzalkonium chloride 0.13% soap

Maa: Yhdysvallat

Kieli: englanti

Lähde: NLM (National Library of Medicine)

Aktiivinen ainesosa:

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

Saatavilla:

Uline

INN (Kansainvälinen yleisnimi):

BENZALKONIUM CHLORIDE

Koostumus:

BENZALKONIUM CHLORIDE 1.3 g in 1 mL

Antoreitti:

TOPICAL

Prescription tyyppi:

OTC DRUG

Käyttöaiheet:

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

Valtuutuksen tilan:

OTC monograph not final

Valmisteyhteenveto

ANTIBACTERIAL- BENZALKONIUM CHLORIDE 0.13% SOAP
ULINE
_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._
----------
ULINE ANTIBACTERIAL HAND SOAP 279.003/279AD
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
wet hands
apply palmful to hands
scrub thoroughly
rinse thoroughly
INACTIVE INGREDIENTS
INACTIVE INGREDIENTS
water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine
oxide, sodium
chloride, myristamidopropylamine oxide, glycerin, fragrance,
disteareth-75 IPDI, PEG-
150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium
benzoate, red
33, red 40, yellow 5
Distributed by:ULINE, 12575 Uline Drive
Pleasant Prairie, WI 53158
1-800-295-5510
uline.com
PRINCIPAL DISPLAY PANEL
ULINE
ANTIBACTERIAL HAND SOAP
S-20661
7.5 FL OZ (221 mL)
ANTIBACTERIAL
benzalkonium chloride 0.13% soap
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:69790-279
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 g
in 1 mL
Uline
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GLYCERIN (UNII: PDC6A3C0OX)
DISTEARETH-75 ISOPHORONE DIIS