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Rexall Maximum Strength

Medically reviewed by Drugs.com. Last updated on Jan 9, 2020.

Dosage form: liquid
Ingredients: BENZOCAINE 20g in 100mL
Labeler: Rexall
NDC Code: 55910-346

Drug Facts

Active ingredient

Benzocaine 20.0% ..................................Purpose: Oral pain reliever

Uses

Temporarily relieves pain associated with the following mouth irritations  toothache sore gums canker sores braces minor dental procedures

Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other “caine” anesthetics

When using this product

  • avoid contact with eyes
  • do not exceed recommended dosage
  • Do not use more than directed for more than 7 days unless directed by a dentist or doctor.

Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days, swelling, rash or fever develops, irritation, pain or redness persists or worsens swelling rash or fever developes

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older:

  • apply to affect4ed area using applicator tip
  • 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: ask a dentist or doctor.

Other Information

Do not use if package has been opened

Store at 20-25°C (68-77°F)

Inactive ingredients

Benzyl Alcohol, D&C Yellow 10, FD&C Blue 1, FD&C Red 40, FD&C Yellow 5, Methylparaben, Flavor, Polyethylene Glycol, Propylene Glycol, Sodium Saccharin, Water

Adults and children 2 years of age and older:
apply to affect4ed area using applicator tip
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: ask a dentist or doctor.

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REXALL  MAXIMUM STRENGTH
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-346
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE20 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
SACCHARIN SODIUM 
METHYLPARABEN 
BENZYL ALCOHOL 
FD&C RED NO. 40 
D&C YELLOW NO. 10 
FD&C BLUE NO. 1 
Product Characteristics
Colororange (dark orange/red to sl brown) Score    
ShapeSize
FlavorMINT (Mint) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:55910-346-691 BOTTLE in 1 CARTON
1NDC:55910-346-6114.7 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35601/01/2015
Labeler - Rexall (068331990)
Registrant - Lornamead (126440440)
Establishment
NameAddressID/FEIOperations
CSR Cosmetic Solutions243501959manufacture(55910-346), pack(55910-346)

 
Rexall

Further information

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