NORTH WOODS DERMA GEL CLEAR- alcohol gel

North Woods Derma Gel Clear by

Drug Labeling and Warnings

North Woods Derma Gel Clear by is a Otc medication manufactured, distributed, or labeled by Superior Chemical Corporation, Betco Corporation, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient

Ethyl Alcohol 70%

Uses

Uses

Hand sanitizer to reduce microorganisms on the skin.

Use this product when soap and water are not available.

Purpose

Purpose

Antiseptic

Warnings

Warnings

For external use only.

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

FLAMMABLE. This product contains ethyl alcohol. Keep away from

sources of ignition.

Discontinue use if irritation or redness develops.

If irritation persists for more than 72 hours, consult a physician.

KEEP OUT OF REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

Read the entire label before using this product.

Place enough product on your palm to thoroughly cover your hands.

Rub hands together briskly until dry.

Inactive Ingredients

Inactive Ingredients

Water, PEG/PPG-8/3 Laurate, Gycerin, Carbomer, Tetrahydroxypropylethylendiamine, Fragrance.

Warnings

KEEP OUT OF REACH OF CHILDREN.

North Woods Derma Gel Clear

INGREDIENTS AND APPEARANCE

NORTH WOODS DERMA GEL CLEAR 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53125-801
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
PROPYLENE OXIDE (UNII: Y4Y7NYD4BK)
ACRYLIC ACID (UNII: J94PBK7X8S)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
LINALOOL (UNII: D81QY6I88E)
HEXYL SALICYLATE (UNII: 8F78EY72YL)
.ALPHA.-PINENE (UNII: JPF3YI7O34)
CYCLOHEXANE (UNII: 48K5MKG32S)
PEG-8 LAURATE (UNII: 762O8IWA10)
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
EDETOL (UNII: Q4R969U9FR)
GERANIOL (UNII: L837108USY)
NEROL (UNII: 38G5P53250)
OCTOXYNOL-13 (UNII: 480KVF3EBY)
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)
CITRONELLOL (UNII: P01OUT964K)
.GAMMA.-TERPINENE (UNII: 4YGF4PQP49)
ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53125-801-57	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2019
2	NDC: 53125-801-04	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2019
3	NDC: 53125-801-09	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2019	08/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/01/2019

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco Corporation, Ltd (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd		005050158	manufacture(53125-801) , label(53125-801)