ECOLAB- alcohol solution

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

Werkstoffen:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Beschikbaar vanaf:

Ecolab Inc.

INN (Algemene Internationale Benaming):

ALCOHOL

Samenstelling:

ALCOHOL 589.4 mg in 1 mL

Toedieningsweg:

TOPICAL

Prescription-type:

OTC DRUG

therapeutische indicaties:

Antiseptic handwash - For handwashing to decrease bacteria on the skin

Autorisatie-status:

OTC monograph not final

Productkenmerken

ECOLAB- ALCOHOL SOLUTION
ECOLAB INC.
----------
DRUG FACTS
ACTIVE INGREDIENT
Ethyl Alcohol 70% w/w
PURPOSE
Antiseptic handwash
USES
For handwashing to decrease bacteria on the skin
WARNINGS
​FOR EXTERNAL USE ONLY
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME, HEAT, SPARKS AND SOURCES OF
STATIC DISCHARGE
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 A DOCTOR IF
Skin irritation or redness occurs 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
Apply product onto hands, spread thoroughly and rub until dry
OTHER INFORMATION
for additional information, see Material Safety Data Sheet (MSDS)
for emergency medical information in USA, call 1 800 328 0026
​INACTIVE INGREDIENTS​ water (aqua), isopropyl alcohol, carbomer,
propylene glycol, tert-
butyl alcohol, aminomethyl propanol, fragrance, denatonium benzoate.
​QUESTIONS? ​call ​1 866 781 8787
PRINCIPAL DISPLAY PANEL AND REPRESENTATIVE LABEL
ECOLAB®
NDC 47593-487-31
GEL HAND SANITIZER
Active Ingredient: 70% w/w Ethyl Alcohol
6000004
NET CONTENTS:
540 ML (18 FL OZ)
This product may be patented: www.ecolab.com/patents
Ecolab - 1 Eclab Place - St. Paul, MN 55102 USA
(c) 2020 Ecolab USA Inc - All rights reserved
Made in United States
www.ecolab.com - 751736/8504/0720
SDS-WI-15014, SDS-NJ-20007, SDS-GA-436
SDS-OK-20022, SDS-IL-20076
ECOLAB
alcohol solution
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:47593-487
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
589.4 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)