COMPOUND BENZOIN TINCTURE- tincture of benzoin liquid

Compound Benzoin Tincture by

Drug Labeling and Warnings

Compound Benzoin Tincture by is a Otc medication manufactured, distributed, or labeled by Medical Chemical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients: Aloe, Benzoin, Storax, Tolu Balsam, Ethanol

PURPOSE

Purpose: Antiseptic

KEEP OUT OF REACH OF CHILDREN

Warnings: Keep out of reach of children.  Ingestion will result in severe gastrointestinal distress, unconsciousness and death.  If ingested induce vomiting if the victim is conscious.  Contact a poison control center immediately.

INDICATIONS & USAGE

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

WARNINGS

Warnings: Keep out of reach of children.  Ingestion will result in a severe gastrointestinal distress, unconsciousness and death.  If ingested induce vomiting if victim is conscious.  Contact a poison control center immediately.

DOSAGE & ADMINISTRATION

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

INACTIVE INGREDIENT

Enter section text here

PRINCIPAL DISPLAY PANEL

benzoinlabel.jpg

INGREDIENTS AND APPEARANCE

COMPOUND BENZOIN TINCTURE 
tincture of benzoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12745-109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOIN RESIN (UNII: GK21SBA74R) (BENZOIN RESIN - UNII:GK21SBA74R)	BENZOIN RESIN	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12745-109-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/1954
2	NDC: 12745-109-02	118 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	06/15/1954
3	NDC: 12745-109-03	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/15/1954

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	06/15/1954

Labeler - Medical Chemical Corporation (008496861)

Establishment
Name	Address	ID/FEI	Business Operations
Medical Chemical Corporation		008496861	manufacture(12745-109)