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Benzocaine by Dynarex Corporation

Medically reviewed on March 22, 2018

Dosage form: swab
Ingredients: BENZOCAINE 0.12mL
Labeler: Dynarex Corporation
NDC Code: 67777-235

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.

Benzocaine Sting & Bite Pad

Active Ingredient

Active Ingredient                             Purpose                  

Benzocaine, 6% w/v                       Topical Analgesic

Isopropyl Alcohol, 70% w/v              Antiseptic

  • For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Keep Out of Reach of Children
  • Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center.

Indications and Usage
  • For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.



  • For external use only.
  • Flammable, keep away from fire or flame.



  • Adults and children 2 years of age and older, apply to affected area 3-4 times daily.
  • Children under 2 years; consult a physician.

Inactive Ingredients
  • Inactive Ingredient: Water.

Do Not UseDo not use: 

  • With electrocautery procedures.
  • In the eyes.

Stop UseStop use:

  • If irritation and redness develop.
  • If condition persists for more than 72 hours, consult a physician.

Storage and Handling
  • Avoid excessive heat.
  • Store at room temperature: 15 - 30 degrees C (59 - 86 degrees F)

Principal Display

Sting and Bite Pad

benzocaine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-235
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:67777-235-013000 PACKET (SWAB) in 1 CASE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34801/24/2011
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)
Taizhou Kanglin Health Protection Products Co Ltd530576131manufacture

Dynarex Corporation

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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.