BENZALKONIUM CHLORIDE liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

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

Available from:

S.P. Richards Company

INN (International Name):

BENZALKONIUM CHLORIDE

Composition:

BENZALKONIUM CHLORIDE 1.3 mg in 1 mL

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antiseptic to decrease bacteria on the skin - irritation or redness develops - condition persists for more than 72 hours

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                BENZALKONIUM CHLORIDE- BENZALKONIUM CHLORIDE LIQUID
S.P. RICHARDS COMPANY
_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._
----------
GENUINE JOE FOAMING HAND SANITIZER (AF)
391
_ACTIVE INGREDIENT_
Benzalkonium chloride 0.13%
_PURPOSE_
Antiseptic
_USE_
to decrease bacteria on the skin
_WARNINGS_
For external use only: hands only
WHEN USING THIS PRODUCT
avoid contact with eyes. If contact occurs, rinse eyes thoroughly with
water.
avoid contact with broken skin
STOP USE AND ASK A DOCTOR IF
irritation or redness develops
condition persists 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_
wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants
_INACTIVE INGREDIENTS_
cetrimonium chloride, diglycerol, disodium cocoamphodiacetate,
fragrance, glycerin,
hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone,
methylchloroisothiazolinone, methylisothiazolinone, tetrasodium EDTA,
water
Distributed by: S.P. Richards Company, Smyrna, GA 30082
www.genuinejoe.com
PRINCIPAL DISPLAY PANEL
Genuine Joe
FOAMING HAND SANITIZER
Alcohol free
14467
8 FL OZ (236 mL)
BENZALKONIUM CHLORIDE
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:62832-118
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1.3 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIGLYCERIN (UNII: 3YC120743U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROCHLORIC ACID (UNII: QTT17582CB)
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M
                                
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