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North Woods Derma Foam Hand Sanitizer

Medically reviewed on October 2, 2017

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Superior Chemical Corporation
NDC Code: 53125-752

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 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

NORTH WOODS DERMA FOAM HAND SANITIZER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53125-752
Route of AdministrationTopicalDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM PYRROLIDONE CARBOXYLATE 
POLYETHYLENE GLYCOL 400 
DIMETHICONE 
DMDM HYDANTOIN 
PEG-3 COCAMINE 
IODOPROPYNYL BUTYLCARBAMATE 
D&C GREEN NO. 5 
Packaging
#Item CodePackage Description
1NDC:53125-752-57550 mL in 1 BOTTLE, PUMP
2NDC:53125-752-541000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/01/2015
Labeler - Superior Chemical Corporation (023335086)
Registrant - Betco corporation, Ltd. (070307547)
Establishment
NameAddressID/FEIOperations
Betco Corporation, Ltd.070307547manufacture(53125-752), pack(53125-752), label(53125-752)

 
Superior Chemical Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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