NORTH WOODS DERMA FOAM E-2- benzalkonium chloride soap

North Woods Derma Foam E-2 by

Drug Labeling and Warnings

North Woods Derma Foam E-2 by is a Otc medication manufactured, distributed, or labeled by Superior Chemical Corporation, Betco corporation, Ltd., Betco Corporation, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

​Active Ingredient

Benzalkonium Chloride 0.13%

INDICATIONS & USAGE

Uses

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

WARNINGS

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.

DOSAGE & ADMINISTRATION

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 INGREDIENT

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

INGREDIENTS AND APPEARANCE

NORTH WOODS DERMA FOAM E-2 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53125-717
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53125-717-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	09/15/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/15/2016

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco corporation, Ltd. (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		024492831	manufacture(53125-717) , label(53125-717) , pack(53125-717)