COMPOUND BENZOIN TINCTURE - benzoin resin liquid 
Medical Chemical Corporation

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.

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Compound Benzoin Tincture Label

Ingredients: Contains aloe, benzoin, storax and tolu balsam dissolved in ethanol.

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.

Keep out of reach of children.  For external use only.  Ingestion will result in severe gastrointestinal distress, unconsciousness and death.  In case of ingestion immediately induce vomiting if the victim is conscious.  Contact a poison control center immediately.

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.

Avoid contact with eyes or mucous membranes.

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.

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Compound Benzoin Tincture Label

COMPOUND BENZOIN TINCTURE 
tincture of benzoin liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:12745-109
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOIN RESIN (BENZOIN RESIN) BENZOIN RESIN10.0 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12745-109-0159 mL in 1 BOTTLE
2NDC:12745-109-02118 mL in 1 BOTTLE, GLASS
3NDC:12745-109-03118 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35606/15/1954
Labeler - Medical Chemical Corporation (008496861)
Establishment
NameAddressID/FEIBusiness Operations
Medical Chemical Corporation008496861manufacture

Revised: 12/2011
Document Id: 3a38e710-73f7-45b8-97b0-7ef38be19718
Set id: 243494ee-342d-4c32-9a86-f8c6c347bd8b
Version: 5
Effective Time: 20111227
 
Medical Chemical Corporation