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Benzoin Compound Tincture by Humco Holding Group, Inc.

Medically reviewed on December 8, 2017

Dosage form: liquid
Ingredients: BENZOIN RESIN 1000mg in 1mL
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-0243

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

Drug Facts

Active Ingredient



Oral mucosal protectant


Forms a coating over wound for protecting recurring canker sores


For external 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.


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 dentist or doctor.

Other information

Flammable: Keep away from spark, heat or flame.

Inactive Ingredients

Alcohol 77%, Aloe, Storax, Tolu Balsam

Principal Display Panel - 16oz

Principal Display Panel - 2 oz

benzoin resin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0243
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:0395-0243-16473 mL in 1 BOTTLE, PLASTIC
2NDC:0395-0243-9259 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35601/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Humco Holding Group, Inc.825672884manufacture(0395-0243), analysis(0395-0243), pack(0395-0243), label(0395-0243)

Humco Holding Group, Inc.

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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.