Benzoin by James Alexander Corporation BENZOIN swab

Benzoin by

Drug Labeling and Warnings

Benzoin by is a Otc medication manufactured, distributed, or labeled by James Alexander Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (each swab)

Benzoin 10%}

Aloe 2%} 

Storax 8%}

Tolu Balsam 4%}

Purpose

Topical bandage adhesive

Uses

An adhesive to hold bandages in place.

Warnings

For external use only.

Allergy alert if you have had a history of contact dermatitis with benzoin compounds.

When using this product avoid getting in the wound.

Stop and ask a doctor if a rash develops.

Flammable liquid Keep away from heat, sparks and open flame.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean and dry skin around the wound. Gently squeeze vial to crush inner ampoule. Allow tincture to saturate the tip of the vial, and carefully apply a thin film of the tincture to the skin on each side of the wound. Allow tincture to dry (30 –40 seconds) before applying bandages.

Other Information

Store at room temperature.

Inactive Ingredients

Alcohol

Questions?

Call 1-908-362-9266, Monday through Friday, 9:00am – 5:00pm e.s.t.

SPL UNCLASSIFIED SECTION

DISPENSING SOLUTIONS®

JAMES ALEXANDER CORPORATION
Blairstown, NJ (908) 362-9266
Product information and MSDS available on-line at:
www.james-alexander.com

Packaging

INGREDIENTS AND APPEARANCE

BENZOIN 
benzoin swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46414-8888
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOIN, (+/-)- (UNII: L7J6A1NE81) (BENZOIN, (+/-) - UNII:L7J6A1NE81)	BENZOIN, (+/-)-	0.6 g  in 0.6 mL
ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9)	ALOE	.12 g  in 0.6 mL
TOLU BALSAM (UNII: TD2LE91MBE) (BALSAM PERU - UNII:8P5F881OCY)	TOLU BALSAM	.24 g  in 0.6 mL
LIQUIDAMBAR STYRACIFLUA RESIN (UNII: P41GWD11CX) (LIQUIDAMBAR STYRACIFLUA RESIN - UNII:P41GWD11CX)	LIQUIDAMBAR STYRACIFLUA RESIN	.48 g  in 0.6 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46414-8888-2	60 mL in 1 BOX; Type 0: Not a Combination Product	10/25/1976

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/25/1976

Labeler - James Alexander Corporation (040756421)

Registrant - James Alexander Corporation (040756421)

Establishment
Name	Address	ID/FEI	Business Operations
James Alexander Corporation		040756421	manufacture(46414-8888)