Product Description.:
Aerosol , clear , clear
Each gram of Kenalog in Orabase provides 1 mg (0.1%) triamcinolone acetonide in emollient dental paste containing gelatin, pectin, and carboboxymethylcellulose sodium in Plastibase? (Plasticized Hydrocarbon Gel), a polyethylene and mineral oil gel base.
ACTIONS
Kenalog (Triamcinolone Acetonide) is a synthetic corticosteroid which possesses anti-inflammatory, antipruritic, and antiallergic action. The emollient dental paste acts as an adhesive vehicle for applying the active medication to the oral tissues. The vehicle provides a protective covering which may serve to temporarily reduce the pain associated with oral irritation.
INDICATIONS
Kenalog in Orabase is indicated for adjunctive treatment and for the temporary relief of symptoms associated with oral inflammatory lesions and ulcerative lesions resulting from trauma.
CONTRAINDICATIONS
This preparation is contraindicated in patients with a history of hypersensitivity to any of its components.
Because it contains a corticosteroid, the preparation is contraindicated in the presence of fungal, viral, or bacterial infections of the mouth or throat.
WARNING
Usage in Pregnancy
Safe use of this preparation during pregnancy has not been established with respect to possible adverse reactions upon fetal development therefore, it should not be used in women of child-bearing potential and particularly during early pregnancy unless, in the judgement of the physician or dentist, the potential benefits outweigh the possible hazards.
PRECAUTIONS
Patients with tuberculosis, peptic ulcer or diabetes mellitus should not be treated with any corticosteroid preparation without the advice of the patient?s physician.
It should be borne in mind that the normal defensive responses of the oral tissues are depressed in patients receiving topical corticosteroid therapy. Virulent strains of oral microorganisms may multiply without producing the usual warning symptoms of oral infections.
The small amount of steroid released when the preparation is used as recommended makes systemic effects very unlikely however, they are a possibility when topical corticosteroid preparations are used over a long period of time.
If local irritation or sensitization should develop, the preparation should be discontinued and appropriate therapy instituted.
If significant regeneration or repair of oral tissues has not occurred in seven days, additional investigation into the etiology of the oral lesion is advised.
ADVERSE REACTIONS
Prolonged administration may elicit the adverse reactions known to occur with systemic steroid preparations for example, adrenal suppression, alteration of glucose metabolism, protein catabolism, peptic ulcer activations, and others. These are usually reversible and disappear when the hormone is discontinued.
