Benzodent description, usages, side effects, indications, overdosage, supplying and lots more!

Benzodent

Chattem, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Benzodent



FULL PRESCRIBING INFORMATION

Drug Facts

Benzocaine 20%

Pain reliever

for the temporary relief of pain due to minor irritation of the mouth and gums caused by dentures or orthodontic appliances or injury to mouth and gums

Allergy alert: Do not use if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other “caine” anesthetics. Localized allergic reactions may occur after prolonged or repeated use.

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

or dentist if

  • sore mouth symptoms do not improve in 7 days
  • swelling, rash or fever develops
  • irritation, pain or redness persists or worsens

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

adults and children 2 years and over:

  • remove cap, break metal seal with cap point
  • apply directly to the gums or to the denture surface that comes in contact with the affected area of the gums
  • if you are using with dentures, wait a few minutes then reinsert dentures and you may use your regular denture adhesive with this product
  • 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: consult a dentist or doctor

cellulose gum, D&C red no. 30 lake, eugenol, FD&C blue no.1 lake, oxyquinoline sulfate, petrolatum (245-003)

Benzocaine 20%
Benzodent®
NET WT 0.25 OZ (7g)
Dental Pain Relieving Cream


Benzodent

Benzocaine CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41167-0053
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOCAINE Benzocaine 0.2 g

Inactive Ingredients

Ingredient Name Strength
CARBOXYMETHYLCELLULOSE SODIUM
Eugenol
OXYQUINOLINE SULFATE
petrolatum
D&C RED NO. 30
FD&C BLUE NO. 1
ALUMINUM OXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 7 in 1 TUBE
2 28 in 1 TUBE
3 NDC:41167-0053-4 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 1994-05-12


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.