Sodium Chloride Injections USP are sterile, nonpyrogenic, isotonic and contain no bacteriostatic or antimicrobial agents These intravenous solutions are indicated for use in adults and pediatric patients as sources of electrolytes and water for hydration PVC-Free and DEHP-Free container It is recommended that the product be stored at room temperature (25°C); however, brief exposure up to 40°C does not adversely affect the product Excel® flexible plastic bag Manufacturer # L8001 Manufacturer B. Braun Country of Origin Unknown Application Replacement Preparation Container Type Flexible Bag Dosage Form IV Solution Generic Drug Code 02962 Generic Drug Name Sodium Chloride, Preservative Free NDC Number 00264780010 Product Dating McKesson Acceptable Dating: we will ship >= 90 days Strength 0.9% Type Intravenous UNSPSC Code 51191602 Volume 500 mL

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Indications Local dental anesthesia by infiltration or nerve block in adults and pediatric patients. Features & benefits Formulation without vaso-constrictor for specific clinical situations.  Fast onset: 30 to 120 seconds in the maxilla and 1 to 4 minutes for the mandible.  Duration: will ordinarily provide pulpal anesthesia of about 20 minutes in the maxilla, and about 40 minutes in the mandible.  No-methylparaben formulation to avoid allergic reactions on sensitive patients.  No natural rubber latex components to help reduce allergic responses.  Terminal sterilization of product/cartridges for safe use.  Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.  Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.  Ordering informationItem #01A1003 – Box containing 5 blisters of 10 x 1.7ml glass cartridges  Safety informationReactions to Scandonest® are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Scandonest® is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of mepivacaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. Scandonest® 2% L contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.  

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Mepivacaine 3% Local Anesthetic PLAIN, Box of 50 - 1.7 mL Cartridges. **Anesthetics are non-returnable.

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