Active Ingredient
Benzocaine 20%
The following Structured Product Label (SPL) was submitted to the FDA by Henry Schein Inc. for the product Benzo Jel (NDC 0404-0018). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, keep out of reach of children., dosage, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzocaine 20%
Oral Anesthetic
Flammable. Do not use near fire or flame. Avoid smoking during use.
Do not use if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics.
Stop use and ask a doctor if
If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center immediately. Avoid spraying in eyes.
A single metered spray dispenses 50 mg of Benzo-Jel Topical Anesthetic. Use only as directed by a dentist.
Store at room temperature. Do not store above 120°F (49°C). Dispose of in a manner consistent with local regulations.
Ethyl Alcohol, Flavor, Polyethelyn Glycol, Sodium Saccharin, Hydrocarbon Propellant (Isobutane and propane).
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