Skip to Content

Benzoin Compound Tincture Professional Pack

Medically reviewed on December 14, 2017.

Dosage form: liquid
Ingredients: BENZOIN RESIN 1000mg in 1mL
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-4209

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.

Humco Benzoin Compound Tincture, USP Professional Pack

Drug Facts

Active Ingredient

Benzoin

Purpose

Pral mucosal protectant

Use

Forms a coating over wound for protecting recurring canker sores

Warnings

For expternal use only. Do not swallow. Do not exceed recommended dosage.

When using this product

Children under 12 years of age should be supervised in the use of this product.

Do not use for more than 7 days unless directed by a dentist or doctor.

Stop use and consult a dentist or doctor if

sore mouth symptoms do not improve in 7 days. irritation, pain or redness persists or worsens. swelling, rash or fever develops.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Adults and children 6 months of age and older: Dry the affected area, with cotton swab, apply undiluted to the affected area not more often than every 2 hours.

Children under 6 months of age: Consult a dentiest or doctor.

Other information

Flammable: Keep away from spark, heat or flame.

Inactive Ingredients

Alcohol 77%, Aloe, Storax, Tolu Balsam

Principal Display Panel - 2 fl oz

Label

BENZOIN COMPOUND TINCTURE PROFESSIONAL PACK 
benzoin resin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-4209
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOIN RESIN (BENZOIN RESIN) BENZOIN RESIN1000 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
ALOE 
TOLU BALSAM 
Packaging
#Item CodePackage Description
1NDC:0395-4209-9259 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35603/25/1998
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(0395-4209), analysis(0395-4209), pack(0395-4209), label(0395-4209)

 
Humco Holding Group, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide