NORTH WOODS DERMA FOAM HAND SANITIZER- benzalkonium chloride soap

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]

ACTIVE INGREDIENT

​Active Ingredient

Benzalkonium Chloride 0.13%

INDICATIONS & USAGE

Uses

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

WARNINGS

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.

DOSAGE & ADMINISTRATION

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 INGREDIENT

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

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

MDS information:​(800) 891-4965

PURPOSE

Purpose

Antiseptic

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Superior Derma Foam Hand Sanitizer.jpg

75229-00_Superior Derma Foam Hand Sanitizer.jpg

INGREDIENTS AND APPEARANCE

NORTH WOODS DERMA FOAM HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53125-700
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
DIOXANE (UNII: J8A3S10O7S)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
HEXYL SALICYLATE (UNII: 8F78EY72YL)
ALCOHOL (UNII: 3K9958V90M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ACETALDEHYDE (UNII: GO1N1ZPR3B)
LIME OIL (UNII: UZH29XGA8G)
LEMON OIL (UNII: I9GRO824LL)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
MYRCENE (UNII: 3M39CZS25B)
DIHYDROMYRCENOL (UNII: 46L1B02ND9)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
WATER (UNII: 059QF0KO0R)
GERANIOL (UNII: L837108USY)
SODIUM PIDOLATE (UNII: 1V74VH163T)
GRAPEFRUIT OIL (UNII: YR377U58W9)
ORANGE OIL (UNII: AKN3KSD11B)
PEG/PPG-15/15 ALLYL ETHER ACETATE (UNII: 8RP39FN7AJ)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53125-700-88	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2015

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

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco corporation, Ltd. (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		005050158	manufacture(53125-700) , pack(53125-700) , label(53125-700)