SYSCO- chloroxylenol solution

Country: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Virkt innihaldsefni:

CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)

Fáanlegur frá:

Ecolab Inc.

INN (Alþjóðlegt nafn):

CHLOROXYLENOL

Samsetning:

CHLOROXYLENOL 0.5 mg in 100 mL

Stjórnsýsluleið:

TOPICAL

Gerð lyfseðils:

OTC DRUG

Ábendingar:

Antiseptic handwash - for handwashing to decrease bacteria on the skin

Leyfisstaða:

OTC monograph not final

Vara einkenni

SYSCO- CHLOROXYLENOL SOLUTION
ECOLAB INC.
----------
DRUG FACTS
ACTIVE INGREDIENT
Chloroxylenol 0.5%
PURPOSE
Antiseptic handwash
USES
for handwashing to decrease bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY
DO NOT USE
in eyes
WHEN USING THIS PRODUCT
if in eyes, rinse promptly and thoroughly with water
discontinue use if irritation and redness develop
STOP USE AND ASK DOCTOR IF
skin irritation or redness occurs for more than 72 hours
KEEP OUR OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
DIRECTIONS
wet hands and forearms
apply 5 ml (teaspoonful) or palmful to hands and forearms
scrub thoroughly for 20 seconds
rinse and repeat
OTHER INFORMATION
for additional information, see Material Safety Data Sheet (MSDS)
for emergency medical information in USA and Canada, call
1.800.328.0026
INACTIVE INGREDIENTS water (aqua), potassium cocoate, hexylene glycol,
sodium
sulfate, tetrasodium EDTA, sodium lauryl sulfate,
hydroxyehtylcellulose, glycerin,
cocoglucoside, glyceryl oleate, citric acid, fragrance,
methylchloroisothiazolinone,
methylisothiazolinone, FDC red 40, FDC yellow 5, DC red 33
QUESTIONS? call 1.800.35.CLEAN (352.5326)
PRINCIPAL DISPLAY PANEL AND REPRESENTATIVE LABEL
SYSCO
RELIANCE SUPC 0279725
SYSCO LIQUID AB HAND SOAP
NET CONTENTS 27.1 US FL OZ (800ML)
DISTRIBUTED BY SYSCO CORPORATION
ECOLAB, 370 WABASHA STREET N, ST PAUL MN 55102-1390 USA, TEL. 1800
352 5326
001123
65100594
751534/5400/0111
SYSCO
chloroxylenol solution
PRODUCT INFORMATION
Ecolab Inc.
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:47593-479
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL -
UNII:0F32U78V2Q)
CHLOROXYLENOL
0.5 mg
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368