North Woods Derma Foam E-2 (Benzalkonium Chloride) Soap [Superior Chemical Corporation] -

NORTH WOODS DERMA FOAM E-2 (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]
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NDC	53125-717-29
Set ID	a91387c8-981e-43c7-a86e-26d02ba90aad
Category	HUMAN OTC DRUG LABEL
Packager	Superior Chemical Corporation
Generic Name
Product Class
Product Number
Application Number	PART333A

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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

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)

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