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Bupivacaine Hydrochloride, Sodium Chloride, Povidone-Iodine, Isopropyl Alcohol

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Overview

What is P-Care MG?

Sodium Chloride Injection, USP, 0.9% is a sterile, nonpyrogenic solution. The osmolarity is 300 mOsmol per liter (calculated).

Each mL contains: Sodium chloride 9 mg; Water for Injection q.s. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single dose containers. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment (pH 4.5-7.0).

Sodium chloride occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. It is soluble in glycerin and slightly soluble in alcohol.

The empirical formula for sodium choride is NaCl and the molecular weight is 58.44.



What does P-Care MG look like?



What are the available doses of P-Care MG?

Sorry No records found.

What should I talk to my health care provider before I take P-Care MG?

Sorry No records found

How should I use P-Care MG?

Gebauer's Pain Ease Medium Stream Spray and Mist Spray are vapocoolants (skin refrigerants) intended for topical application to skin, intact mucous membranes (oral cavity, nasal passage ways and the lips) and minor open wounds. Pain Ease instantly controls pain associated with injections (venipuncture, IV starts, cosmetic procedures), minor surgical procedures (such as lancing boils, incisions, drainage of small abscesses and sutures) and the temporary relief of minor sports injuries (sprains, bruising, cuts and abrasions).

Wipe injection site vigorously and discard


What interacts with P-Care MG?

Sorry No Records found


What are the warnings of P-Care MG?

Sorry No Records found


What are the precautions of P-Care MG?

Sorry No Records found


What are the side effects of P-Care MG?

Sorry No records found


What should I look out for while using P-Care MG?

Pain Ease is contraindicated in individuals with a history of hypersensitivity to 1,1,1,3,3-Pentafluoropropane and 1,1,1,2-Tetrafluoroethane. If skin irritation develops, discontinue use.

For external use only. Contents under pressure. For use on minor open wounds only.For use on intact mucous membranes only.

KEEP OUT OF REACH OF CHILDREN


What might happen if I take too much P-Care MG?

When used as a diluent, solvent or intravascular flushing solution, this parenteral preparation is unlikely to pose a threat of sodium chloride or fluid overload except possibly in very small infants.  In the event these should occur, reevaluate the patient and institute appropriate corrective measures.  (See and ).


How should I store and handle P-Care MG?

Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F). [See USP Controlled Room Temperature.]Aerosol CanGebauer’s Pain Ease® Medium Stream Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-031.0 fl. oz. (30mL) - P/N 0386-0008-04 Gebauer’s Pain Ease® Mist Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-021.0 fl. oz. (30mL) - P/N 0386-0008-01For more information about this product contact Gebauer Company.Aerosol CanGebauer’s Pain Ease® Medium Stream Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-031.0 fl. oz. (30mL) - P/N 0386-0008-04 Gebauer’s Pain Ease® Mist Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-021.0 fl. oz. (30mL) - P/N 0386-0008-01For more information about this product contact Gebauer Company.Aerosol CanGebauer’s Pain Ease® Medium Stream Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-031.0 fl. oz. (30mL) - P/N 0386-0008-04 Gebauer’s Pain Ease® Mist Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-021.0 fl. oz. (30mL) - P/N 0386-0008-01For more information about this product contact Gebauer Company.Aerosol CanGebauer’s Pain Ease® Medium Stream Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-031.0 fl. oz. (30mL) - P/N 0386-0008-04 Gebauer’s Pain Ease® Mist Spray 3.5 fl. oz. (103.5mL) - P/N 0386-0008-021.0 fl. oz. (30mL) - P/N 0386-0008-01For more information about this product contact Gebauer Company.


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Sodium chloride in water dissociates to provide sodium (Na+) and chloride (Cl—) ions. These ions are normal constituents of the body fluids (principally extracellular) and are essential for maintaining electrolyte balance.

The distribution and excretion of sodium (Na+) and chloride (Cl—)are largely under the control of the kidney which maintains a balance between intake and output.

The small volume of fluid and amount of sodium chloride provided by Sodium Chloride Injection, USP, 0.9%, when used only as a vehicle for parenteral injection of drugs, is unlikely to exert a significant effect on fluid and electrolyte balance except possibly in very small infants.

Water is an essential constituent of all body tissues and accounts for approximately 70% of total body weight. Average normal adult daily requirement ranges from two to three liters (1 to 1.5 liters each for insensible water loss by perspiration and urine production).

Water balance is maintained by various regulatory mechanisms. Water distribution depends primarily on the concentration of electrolytes in the body compartments and sodium (Na+) plays a major role in maintaining physiologic equilibrium.

Non-Clinical Toxicology
Pain Ease is contraindicated in individuals with a history of hypersensitivity to 1,1,1,3,3-Pentafluoropropane and 1,1,1,2-Tetrafluoroethane. If skin irritation develops, discontinue use.

For external use only. Contents under pressure. For use on minor open wounds only.For use on intact mucous membranes only.

KEEP OUT OF REACH OF CHILDREN

1. Do not spray in the eyes.

2. Do not use this product on persons with poor circulation or insensitive skin.

3. When used to produce local freezing of tissues, adjacent skin areas should be protected by an application of petroleum.

4. The freezing and thawing process may be painful, and freezing may lower local resistance to infection and delay healing.

5. Over application of the product might cause frostbite and/or after skin pigmentation.

6. Do not use on large areas of damaged skin, puncture wounds, animal bites or serious wounds.

7. Apply only to intact mucous membranes.

8. Do not use on genital mucous membranes.

Freezing can occasionally alter skin pigmentation.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

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