HYDRO KLEEN AF- benzalkonium chloride liquid

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

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01-08-2014

Wirkstoff:

Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Verfügbar ab:

Productive Practices

INN (Internationale Bezeichnung):

Benzalkonium Chloride

Zusammensetzung:

Benzalkonium Chloride 0.13 g in 1 mL

Verabreichungsweg:

TOPICAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

Antibacterial - Provide hand sanitizing when soap and water not available - Kills or reduces 99.9% of harmful bacteria/germs - Recommended for repeated use

Berechtigungsstatus:

OTC monograph not final

Fachinformation

                                HYDRO KLEEN AF- BENZALKONIUM CHLORIDE LIQUID
PRODUCTIVE PRACTICES
_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._
----------
HYDRO KLEEN AF
_DRUG FACTS_
ACTIVE INGREDIENT
Benzalkonium Chloride 0.13%
PURPOS E
Antibacterial
US ES
Provide hand sanitizing when soap and water not available
Kills or reduces 99.9% of harmful bacteria/germs
Recommended for repeated use
WARNINGS
For external use only
Do not use in or near the eyes
In case of contact with eyes, flush thoroughly with water
If ingested, consult with a physician
Keep out of range of children 2yrs of age or younger
DIRECTIONS
Apply thumbnail size amount to palm
Rub hands together thoroughly
No rinsing required
OTHER INFORMATION
Do not freeze
INACTIVE INGREDIENTS
Water, Polysorbate 20, Glycerin, Citric Acid, Butylene Glycol,
Cocamidopropylamine Oxide, Sodium
Hydroxide, Cocamidopropyl Betaine, Cetrimonium Chloride
QUES TIONS ?
1-877-446-8088 • www.ProductivePractices.net
PRINCIPAL DISPLAY PANEL - 200 ML BOTTLE LABEL
ALCOHOL-FREE
HYDROKLEENAF
HAND SANITIZER
ANTISEPTIC
ANTI-BACTIERIAL
DYE FREE
FRAGRANCE FREE
DISTRIBUTED BY
6.7 fl oz (200ml)
HYDRO KLEEN AF
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 9 129 -0 10
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
BENZA LKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6
JUD5X6 Y)
Benzalko nium Chlo ride
0 .13 g in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WA TER (UNII: 0 59 QF0 KO0 R)
PO LYSO RBA TE 2 0 (UNII: 7T1F30 V5YH)
GLYCERIN (UNII: PDC6 A3C0 OX)
CITRIC ACID MO NO HYDRA TE (UNII: 29 6 8 PHW8 QP)
BUTYLENE GLYCO L (UNII: 3XUS8 5K0 RA)
CO CA MIDO PRO PYLA MINE O XIDE (UNII: M4SL8 2J7HK)
SO DIUM HYDRO XIDE (UNII: 55X0 4QC32I)
CO CA MIDO PRO PYL BETA INE (UNII: 5OCF3O11KX)
CETRIMO NIUM CHLO RIDE (UNII: UC9 PE9 5IBP)
Pr
                                
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