ANTIBACTERIAL HAND CLEANSER- benzalkonium chloride soap

Država: Združene države Amerike

Jezik: angleščina

Source: NLM (National Library of Medicine)

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Prenos Lastnosti izdelka (SPC)
24-08-2023

Aktivna sestavina:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Dostopno od:

Kimball Midwest

Pot uporabe:

TOPICAL

Tip zastaranja:

OTC DRUG

Terapevtske indikacije:

Uses Handwash to help decrease bacteria on skin. Purpose Antibacterial Handwashing

Status dovoljenje:

OTC monograph not final

Lastnosti izdelka

                                ANTIBACTERIAL HAND CLEANSER- BENZALKONIUM CHLORIDE SOAP
KIMBALL MIDWEST
_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._
----------
KIMBALL MIDWEST F215F
DOSAGE AND ADMINISTRATION
DIRECTIONS Apply a small amount, covering hands with product for 30
seconds. Add
water, lather and rinse.
Children under 6 years of age should be supervised when using this
product.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS Water, Cetrimonium Chloride, Lauramine Oxide,
Sorbitol,
Cocamide MEA, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Sodium
Lauraminodipropionate, Citric Acid, Fragrance, Disodium EDTA,
Methyllisothiazolinone,
Methylchloroisothiazolinone, Yellow 5, Red 33
INDICATIONS AND USAGE SECTION
USES Handwash to help decrease bacteria on skin.
KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or
contact a Poison
Control Center right away.
PURPOSE SECTION
PURPOSE Antibacterial Handwashing
ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENT Benzalkonium Chloride 0.13% w/w
WARNINGS SECTION
WARNINGS
FOR EXTERNAL USE ONLY.
DO NOT USE in eyes. In case of contact, immediately flush with water.
STOP USE AND ASK A DOCTOR IF irritation or rash appears and lasts.
PRINCIPAL DISPLAY LABEL
ANTIBACTERIAL HAND CLEANSER
benzalkonium chloride soap
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:66608-215
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
0.013 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ACID RED 35 (UNII: 02BXM5Q7GE)
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (
                                
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