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laboratorios alfa srl - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698), sodium lactate (unii: tu7hw0w0qt) (lactic acid - unii:33x04xa5at), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152), calcium chloride (unii: m4i0d6vv5m) (calcium cation - unii:2m83c4r6zb) - veterinary lactated ringer’s injection, usp is indicated as a source of water and electrolytes or as an alkalinizing agent. veterinary lactated ringer’s injection, usp is contraindicated in patients with a known hypersensitivity to sodium lactate. this is a single dose container and does not contain preservatives. use the solution immediately after the bottle is opened, discard the remaining one. squeeze and inspect the bottle, discard if leaks are found or if the solution contains visible and solid particles. do not administer simultaneously with blood. do not use it unless solution is clear and seal is intact, the solution containing dextrose may be contraindicated in patients with a known allergy to corn or corn products. directions for use plastic container: preparation and administration 1. check for minute leaks by squeezing the container firmly. if leaks are found, discard solution as sterility may be impaired. 2. suspend container from eyelet support. 3. remove plastic protector from ports area at the bottom of container. 4. hold the bottle in vertical position and inset pyrogen free iv administration set in the outlet port. use aseptic technique to add medication warning: additives may be incompatible. to add medication before solution administration 1. prepare medication site. 2. using syringe with 18 to 21 gauge needle, puncture inlet port and inject. 3. mix solution and medication thoroughly. for high density medication such as potassium chloride, squeeze ports while ports are upright and mix thoroughly. to add medication during solution administration 1. close clamp on the set. 2. prepare medication site. 3. using syringe with 18 to 21 gauge needle, puncture inlet port and inject. 4. remove container from iv pole and/or turn to an upright position. 5. mix solution and medication thoroughly. 6. return container to in use position and continue administration. caution: federal law (usa) restricts this drug to use by or on the order of a licensed veterinarian.

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hyland's - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698), strychnos nux-vomica seed (unii: 269xh13919) (strychnos nux-vomica seed - unii:269xh13919), phosphorus (unii: 27ylu75u4w) (phosphorus - unii:27ylu75u4w), anemone pulsatilla (unii: i76kb35jev) (anemone pulsatilla - unii:i76kb35jev), sulfur (unii: 70fd1kfu70) (sulfur - unii:70fd1kfu70), onion (unii: 492225q21h) (onion - unii:492225q21h), coffee bean (unii: jfh385y744) (coffee bean - unii:jfh385y744), chamomile (unii: fgl3685t2x) (cha - sodium chloride 6 [hp_x] in 1 ml - temporarily relieves the symptoms of the common cold including cough, runny nose,sneezing, nasal and chest congestion, and sore throat with accompanying occasional sleeplessness.

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b. braun medical inc. - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium cation 0.9 g in 100 ml - 0.9% sodium chloride irrigation usp is indicated for all general irrigation, washing, rinsing and dilution purposes which permit use of a sterile, nonpyrogenic electrolyte solution. 0.9% sodium chloride irrigation usp is not for injection by usual parenteral routes. an electrolyte solution should not be used for irrigation during electrosurgical procedures.

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fresenius kabi usa, llc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular, or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.

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hikma pharmaceuticals usa inc. - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - this parenteral preparation indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered. 

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sypharma pty ltd - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698, sodium cation - unii:lyr4m0nh37), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152, chloride ion - unii:q32zn48698), calcium chloride (unii: m4i0d6vv5m) (calcium cation - unii:2m83c4r6zb, chloride ion - unii:q32zn48698), sodium lactate (unii: tu7hw0w0qt) (lactic acid - unii:33x04xa5at, sodium cation - unii:lyr4m0nh37) - sodium chloride 600 mg in 100 ml - sykes lactated ringer’s injection is indicated as a source of water and electrolytes for all species. it is also used as an alkalinizing agent. sykes lactated ringer’s injection is contraindicated in patients with a known hypersensitivity to sodium lactate; congestive heart failure or severe impairment of renal function; clinical states in which the administration of sodium and chloride is detrimental.

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it3 medical llc - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698) - these parenteral preparations are indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.  not for inhalation . due to potential toxicity of benzyl alcohol in newborns, bacteriostatic sodium chloride injection, usp, 0.9% containing benzyl alcohol must not be used in this patient population. bacteriostatic sodium chloride injection, usp, 0.9% should not be used for fluid or sodium chloride replacement.

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leosons overseas corp - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698, sodium cation - unii:lyr4m0nh37) - - for dry nasal membranes

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cvs pharmacy - sodium bicarbonate (unii: 8mdf5v39qo) (bicarbonate ion - unii:hn1zra3q20), sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698) - sodium bicarbonate 22.8 mg in 100 mg - purpose nasal wash uses temporarily relieves symptoms associated with sinusitus, cold, flu or allegies: -sneezing -nasal stuffiness -runny nose -post nasal drip removes inhaled irritants (dust, pollen) helps to loosen thick mucous moistens nasal passages instructions for use: directions: read through entire section before using for the first time. 1. empty the contents of one instant relief sinus wash packet into the sinus wash neti pot. first-time users should start with 1/2 packet of the dry ingredients. as you become more accustomed to the system, work up to using 1 full packet. additional packets may be purchased from your nearest pharmacy. 2. fill the pot halfway or to the middle of the indentation with proper water.this makes 1/2 cup (4 oz.) solution. 3. stir thoroughly until dry ingredients have completely dissolved. 4. proper head position allows solution to run through the nose by gravity. -lean over the sink with your head bent down so you are looking directly into the basin. holding the pot in your right hand, gently insert the spout into your right nostril so that it forms a comfortable seal. -rotate your head so that the right nostril is directly above the left. the forehead should remain higher than the chin. raise the handle of the pot so that the solution enters the right nostril. in a few moments, the solution will begin to drain out of the left nostril into the sink. do not inhale or "snort" solution into the nose-breathe through your mouth. 5. when the pot is empty, exhale through both nostrils to clear them of excess mucus and solution. gently blow your nose into a tissue. 6. repeat the procedure on the other side. 7. thoroughly rinse the pot after each use with water that has been distilled, sterilized, filtered or previously boiled and leave the pot to air dry completely. the instant relief sinus wash neti pot is top-rack dishwasher safe.

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hospira, inc. - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698, sodium cation - unii:lyr4m0nh37) - this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered. due to the potential toxicity of benzyl alcohol in neonates, solutions containing benzyl alcohol must not be used in this patient population. parenteral preparations with benzyl alcohol should not be used for fluid or sodium chloride replacement. parenteral preparations containing benzyl alcohol should not be used in epidural or spinal anesthetic procedures.