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.

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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

71729-00 Superior Derma Foam E2

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

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

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

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

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

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco corporation, Ltd. (024492831)

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