Opahl gel

Active ingredient

Benzocaine, 20%


Oral anesthetic


For the temporary relief of pain associated with canker sores and minor dental procedures


Allergy alertDo not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "-caine" anesthetics.

Do not use

this product for more than 7 days unless directed by a dentist or doctor. If sore mouth symptoms do not improve in 7 days; if irritation, pain, or redness persists or worsens; or if swelling, rash, or fever develops, see your dentist or doctor promptly.

Do not

exceed recommended dosage

Keep out of reach of children

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


  • Adults and children 2 years of age and older: Apply to the affected area. 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 2 years of age: Consult a dentist or doctor.

Other information

Store at room temperature 59-86F (15-30C). Protect from freezing and heat.

Inactive ingredients

FD&C Red #40, Flavor, Polyethylene glycol 3350, Polyethylene glycol 400, Saccharine sodium, Tocopheryl acetate, Xylitol, Water

Ingredients and appearance - Product information

Opahl gel- Benzocaine

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 53045-100
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Benzocaine ( UNII: U3RSY48JW5)( Benzocaine - UNII: U3RSY48JW5 ) 6.4 gin 32 g

Inactive Ingredients

Ingredient Name Code
Fd&c red no. 40 ( UNII: WZB9127XOA)
Polyethylene glycol 3350 ( UNII: G2M7P15E5P)
Polyethylene glycol 400 ( UNII: B697894SGQ)
Saccharin sodium ( UNII: SB8ZUX40TY)
.alpha.-tocopherol acetate ( UNII: 9E8X80D2L0)
Xylitol ( UNII: VCQ006KQ1E)
Water ( UNII: 059QF0KO0R)

Product Characteristics


Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part356 USA

Labeler - Dharma Research, Inc.( 078444642)


Name ID/FEI Business Operations
Dharma Research, Inc. 078444642 manufacture( 53045-100)


Oral Anesthetic Gel Bubble Gum

with Vitamin E and Xylitol

Gluten Free

1.12 oz (32 g)

Manufactured by Dharma Research, Inc., 5220 NW 72nd Ave, Unit 15, Miami, FL 33166



NDC: 53045-100-30