PURELL ADVANCED SOOTHING- alcohol gel

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Compra

Scarica Scheda tecnica (SPC)
16-12-2022

Principio attivo:

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

Commercializzato da:

GOJO Industries, Inc.

Via di somministrazione:

TOPICAL

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

Antimicrobial - Hand sanitizer to help reduce bacteria on the skin

Stato dell'autorizzazione:

OTC monograph not final

Scheda tecnica

                                PURELL ADVANCED SOOTHING- ALCOHOL GEL
GOJO INDUSTRIES, INC.
_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._
----------
PURELL ADVANCED HAND SANITIZER SOOTHING GEL
ACTIVE INGREDIENT
Ethyl alcohol 70% v/v
PURPOSE
Antimicrobial
USES
Hand sanitizer to help reduce bacteria on the skin
WARNINGS
FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.
FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT do not use in or near the eyes. In case of
contact, rinse
eyes thoroughly with water.
STOP USE AND ASK A DOCTOR if irritation or rash appears and lasts
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
DIRECTIONS
Put enough product in your palm to cover hands and rub hands together
briskly until
dry
Children under 6 years of age should be supervised when using PURELL
INACTIVE INGREDIENTS
Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl
Glycol, Glycerin,
Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl
Acrylate Crosspolymer,
Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5
(CI 19140)
Distributed by: GOJO Industries, Inc. Akron, OH 44309
Questions? Tel: 1-888-4-PURELL
www.PURELL.com
©2011, GOJO Industries, Inc.
All rights reserved. Made in U.S.A.
PURELL ADVANCED SOOTHING
alcohol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:21749-713
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
0.7 mL in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626
                                
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