Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED PerioGard® is supplied as a blue liquid in a 16-fluid ounce (473 mL) (NDC 0126-0282-16) amber plastic bottle with child-resistant dosage cap. Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Rx Only. Keep out of reach of children.; PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label Colgate ® NDC 0126-0282-16 PerioGard ® (Chlorhexidine Gluconate Oral Rinse USP, 0.12%) ALCOHOL FREE Rx Only PLACE PHARMACY LABEL HERE Dispense in original container or in amber glass. KEEP OUT OF REACH OF CHILDREN For questions or comments contact your dentist or pharmacist. 16 FL OZ (1 PT) 473 mL PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
- HOW SUPPLIED PerioGard® is supplied as a blue liquid in a 16-fluid ounce (473 mL) (NDC 0126-0282-16) amber plastic bottle with child-resistant dosage cap. Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Rx Only. Keep out of reach of children.
- PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label Colgate ® NDC 0126-0282-16 PerioGard ® (Chlorhexidine Gluconate Oral Rinse USP, 0.12%) ALCOHOL FREE Rx Only PLACE PHARMACY LABEL HERE Dispense in original container or in amber glass. KEEP OUT OF REACH OF CHILDREN For questions or comments contact your dentist or pharmacist. 16 FL OZ (1 PT) 473 mL PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
Overview
PerioGard® (Chlorhexidine Gluconate Oral rinse USP, 0.12%) is an oral rinse containing 0.12% chlorhexidine gluconate (1,1'-hexamethylene bis [5-(p-chlorophenyl) biguanide] di-D-gluconate) in a base containing water, propylene glycol, glycerin, sorbitol, polyoxyl 40 hydrogenated castor oil, flavor, cetylpyridinium chloride, and FD&C blue no. 1. PerioGard® product is a near neutral solution (pH range 5-7). Chlorhexidine gluconate is a salt of chlorhexidine and gluconic acid. Its chemical structure is: Chemical Structure
Indications & Usage
PerioGard® (Chlorhexidine Gluconate Oral Rinse USP, 0.12%) is indicated for use between dental visits as part of a professional program for the treatment of gingivitis as characterized by redness and swelling of the gingivae, including gingival bleeding upon probing. PerioGard® has not been tested among patients with acute necrotizing ulcerative gingivitis (ANUG). For patients having coexisting gingivitis and periodontitis, see PRECAUTIONS .
Dosage & Administration
PerioGard® (Chlorhexidine Gluconate Oral Rinse USP, 0.12%) therapy should be initiated directly following a dental prophylaxis. Patients using PerioGard® should be reevaluated and given a thorough prophylaxis at intervals no longer than six months. Recommended use is twice daily oral rinsing for 30 seconds, morning and evening after toothbrushing. Usual dosage is 1/2 fl. oz. ("15 mL" line in dosage cap) of undiluted PerioGard®. Patients should be instructed not to rinse with water or other mouthwashes, brush teeth, or eat immediately after using PerioGard®. PerioGard® is not intended for ingestion and should be expectorated after rinsing.
Warnings & Precautions
WARNINGS The effect of PerioGard® on periodontitis has not been determined. An increase in supragingival calculus was noted in clinical testing with users of chlorhexidine gluconate oral rinse USP, 0.12% compared with control users. It is not known if chlorhexidine gluconate use results in an increase of subgingival calculus. Calculus deposits should be removed by a dental prophylaxis at intervals not greater than six months. Anaphylaxis, as well as serious allergic reactions, have been reported during postmarketing use with dental products containing chlorhexidine. SEE CONTRAINDICATIONS .
Contraindications
PerioGard® should not be used by persons who are known to be hypersensitive to chlorhexidine gluconate or other formula ingredients.
Adverse Reactions
The most common side effects associated with chlorhexidine gluconate oral rinse USP, 0.12% are: (1) an increase in staining of teeth and other oral surfaces, (2) an increase in calculus formation, and (3) an alteration in taste perception; see WARNINGS and PRECAUTIONS . Oral irritation and local allergy-type symptoms have been spontaneously reported as side effects associated with use of chlorhexidine gluconate rinse. The following oral mucosal side effects were reported during placebo-controlled adult clinical trials: aphthous ulcer, grossly obvious gingivitis, trauma, ulceration, erythema, desquamation, coated tongue, keratinization, geographic tongue, mucocele, and short frenum. Each occurred at a frequency of less than 1.0%. Among postmarketing reports, the most frequently reported oral mucosal symptoms associated with chlorhexidine gluconate oral rinse USP, 0.12% are stomatitis, gingivitis, glossitis, ulcer, dry mouth, hypesthesia, glossal edema, and paresthesia. Minor irritation and superficial desquamation of the oral mucosa have been noted in patients using chlorhexidine gluconate oral rinse. There have been cases of parotid gland swelling and inflammation of the salivary glands (sialadenitis) reported in patients using chlorhexidine gluconate oral rinse.
Storage & Handling
Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Rx Only. Keep out of reach of children.
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