NORTH WOODS DERMA FOAM E-2- benzalkonium chloride soap

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:

Superior Chemical Corporation

INN (International Name):

BENZALKONIUM CHLORIDE

Composition:

BENZALKONIUM CHLORIDE 1.3 mg in 1 mL

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Uses - For handwashing to decrease the bacteria on the skin. - Recommended for repeated use.

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                NORTH WOODS DERMA FOAM E-2- BENZALKONIUM CHLORIDE SOAP
SUPERIOR CHEMICAL CORPORATION
_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._
----------
NORTH WOODS DERMA FOAM E-2
_ACTIVE INGREDIENT_
Benzalkonium Chloride 0.13%
_USES_
For handwashing to decrease the bacteria on the skin.
Recommended for repeated use.
_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 persists or redness deelops,
or if 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_
READ THE ENTIRE LABEL BEFORE USING THIS PRODUCT.
Dispense 2 pumps of product onto palm of hand and scrub thoroughly
over all surfaces of both
hands for 15 seconds. Rinse with clean water.
_INACTIVE INGREDIENTS_
Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine
oxide, citric acid.
SUPERIOR DERMA FOAM E2
_PURPOSE_
Antimicrobial
SUPERIOR DERMA FOAM E2
KEEP OUT OF REACH OF CHILDREN
SUPERIOR DERMA FOAM E2
71729-00 Superior Derma Foam E2
NORTH WOODS DERMA FOAM E-2
benzalkonium chloride soap
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:53125-717
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
1.3 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
CO CO GLUCO SIDE (UNII: ICS79 0 225B)
LAURTRIMO NIUM CHLO RIDE (UNII: A8 1MSI0 FIC)
CO CAMIDO PRO PYLAMINE O XIDE (UNII: M4SL8 2J7HK)
CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)
Superior Chemical Corporation
CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING S
                                
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