North Woods Derma Foam Hand Sanitizer

North Woods Derma Foam Hand Sanitizer by

Drug Labeling and Warnings

North Woods Derma Foam Hand Sanitizer 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]

NORTH WOODS DERMA FOAM HAND SANITIZER- benzalkonium chloride soap 
Superior Chemical Corporation

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North Woods Derma Foam Hand Sanitizer

​Active Ingredient

Benzalkonium Chloride 0.13%

Uses

• Use in a variety of public facilities.
• Use this product when soap and water are not available.

Warnings

• For external use only.
• Avoid contact with eyes.
• Children under the age of 6 should be supervised by an adult when using this product.
• Discontinue use is irritation or redness develops.
• If irritation persists for more than 72 hours, consult a physician.
• KEEP OUT OF REACH OF CHILDREN.

Directions

• ​Read the entire label before using this product.
• ​Dispense product onto dry hands. Rub hands together until hands are dry.
• Use as needed between hand washes to reduce bacteria on the skin.

Inactive Ingredients

Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Purpose

Antiseptic

KEEP OUT OF REACH OF CHILDREN

Superior Derma Foam Hand Sanitizer.jpg

75229-00_Superior Derma Foam Hand Sanitizer.jpg

NORTH WOODS DERMA FOAM HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53125-752
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)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PEG-3 COCAMINE (UNII: KTM00873VC)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53125-752-57	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2015	04/01/2019
2	NDC: 53125-752-54	1000 mL in 1 BAG; Type 0: Not a Combination Product	10/01/2015	04/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/01/2015	04/01/2019

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco corporation, Ltd. (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		005050158	manufacture(53125-752) , pack(53125-752) , label(53125-752)

Revised: 12/2024

Document Id: 2a3a53ef-c248-a09b-e063-6394a90a2d8b

34390-5

Set id: 42504bc7-bcf6-4338-b640-44fcb51f72cc

Version: 8

Effective Time: 20241226