AFIA FOAMING ANTI-BACTERIAL HAND CLEANER- chloroxylenol soap

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

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Preparatomtale Preparatomtale (SPC)
28-10-2022

Aktiv ingrediens:

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

Tilgjengelig fra:

National Chemical Laboratories, Inc.

Administreringsrute:

TOPICAL

Resept typen:

OTC DRUG

Indikasjoner:

For hand washing to decrease bacteria on the skin For hand washing to decrease bacteria on the skin

Autorisasjon status:

OTC monograph not final

Preparatomtale

                                AFIA FOAMING ANTI-BACTERIAL HAND CLEANER- CHLOROXYLENOL SOAP
NATIONAL CHEMICAL LABORATORIES, 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._
----------
LISTING OF AFIA FOAMING ANTI-BACTERIAL HAND CLEANER
DRUG FACTS
ACTIVE INGREDIENT. PURPOSE
Chloroxylenol 0.3%............Antimicrobial
USES
For hand washing to decrease bacteria on the skin
WARNINGS:
FOR EXTERNAL USE ONLY.
WHEN USING THIS PRODUCT avoid contact with eyes. In case of eye
contact, flush eyes
with water.
STOP USE AND ASK A DOCTOR if irritation or redness develops, or if
condition persists
for more than 72 hours.
DIRECTIONS
Wet a hand. Pump one or two stokes of foam, into palm of hand.
Rub thoroughly over all surfacesof both hands for 30 seconds
Rinse hands and dry thoroughly.
INACTIVE INGREDIENTS
Water, Sodium Methyl 2-Sulfolaurate, Disodium 2-Sulfolaurate, Decyl
glucoside,
Cocamidopropyl Betaine, Lauric Monoethanolamide, Cetrimonium Chloride,
PEG-150
Distearate, Phenoxyethanol, fragrance, Methylchloroisothiazolinone,
Methylisothiazolinone, FD&C yellow #5, FD&C blue #1
WARNINGS:
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control
Center right away.
USES
For hand washing to decrease bacteria on the skin
AFIA FOAMING ANTI-BACTERIAL HAND CLEANER
chloroxylenol soap
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:71023-446
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)
CHLOROXYLENOL
3 mg in 1 mL
INACTIVE INGREDIENTS
National Chemical Laboratories, Inc.
INGREDIENT NAME
STRENGTH
LAURIC MONOETHANOLAMIDE (UNII: 098P2IGT76)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX
                                
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