Skip to main content


Dosage form: gel
Ingredients: BENZOCAINE 20g in 100g
Labeler: Dr. Fresh LLC
NDC code: 64893-385

Medically reviewed by Last updated on Jan 4, 2024.


Drug Fcats

Active Ingredient

Benzocaine 20%


Oral Pain Reliever


for the temporary relief of pain due to toothaches.


For external use only.

Allergy Alert: do not use the product if you havd a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics.

Do not use

for more than 7 days unless recommended by a dentist or doctor.

Stop use and ask a doctor if

swelling, rash or fever develops - irritation, pain or redness persists or worsens

Keep out of reach of children.

If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away.


Wash hands - remove pen cap - twist the bottom several times until the brush tip is covered with the gel.

Adults and children 6 years of age and older: Apply a small amount of product to the cavity and around the gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or doctor.  Children under 12 years of age - Should be supervised in the use of this product. Children under 6 years of age: Ask a dentist or doctor.

Other Information

Do not use if pen or package  has been opened. This preparation is intended for use in case of toothache, only as a temporary expedient until a dentist can b consulted. Do not use continuously. This formula will stay in place for an extended duration for relief.

Inactive Ingredients

Flavor, Glycerin, Polyethylene Glycol, Polyvinyl Pyrrolidone, Sorbic Acid, Sucralose, Red No. 40

Package Labeling:

benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64893-385
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
#Item CodePackage Description
1NDC:64893-385-022 g in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35609/26/2011
Labeler - Dr. Fresh LLC (117376803)

Dr. Fresh LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.