Phone: 908-362-9266
Fax: 908-362-5019
845 Route 94, Blairstown, NJ 07825
Amyl Nitrite Inhalant USP is an organic nitrite used for the relief and prophylactic management of angina pectoris. The drug is delivered via inhalation.
The principal pharmacological action of Amyl Nitrite is relaxation of vascular smooth muscle, resulting in generalized vasodilation. Although Amyl Nitrite reflexly increases heart rate and myocardial contractility which increases myocardial oxygen consumption, the reduction in ventricular wall tension results in a net decrease in myocardial oxygen consumption. By decreasing myocardial oxygen consumption, Amyl Nitrite alters the imbalance of myocardial oxygen supply which causes angina pectoris.
James Alexander’s Amyl Nitrite Inhalant USP carries an expiration date of three years.
Keep protected from light at 2-8 degrees C (36-46 degrees F). Amyl Nitrite is extremely flammable. Keep from heat and open flame.
The inhalant should be held away from the face while activating the package. To break the inner vial, crush ONCE between the thumb and forefinger at the dot located at the center of the inhalant. Carefully pass the inhalant back and forth close to the nose of the affected person several times. Discard inhalant after use. Relief usually occurs in one to three minutes.
Amyl Nitrite Inhalant is a prescription drug. Use only in accordance with a physician’s instructions. FDA regulations specifically prohibit labeling the product for uses other than the treatment of angina pectoris (see 21CFR 250.102)
JAC offers Amyl Nitrite Inhalant USP as a unit dose inhalant containing 0.3 mls. The inhalants are packaged in the following configurations:
James Alexander Corporation’s Ammonia Inhalant Solution is a proprietary formulation used to prevent or treat fainting.
The active ingredient in Ammonia Inhalant is Strong Ammonia Solution NF. The formulation is precisely adjusted to yield an ammonia concentration of 18.5% w/w. The formulation also contains 35.0-40.0% v/v Dehydrated Alcohol USP.
James Alexander’s Ammonia Inhalants fully meet the U.S. Government’s specification number U-A-500B dated March 30, 1976 for Aromatic Ammonia Inhalants.
James Alexander’s Ammonia Inhalants carry a five (5) year expiration date, the maximum allowed by the Food and Drug Administration.
Ammonia Inhalants are used for inhalation only to prevent or treat fainting. The inhalant should be held away from the face while activating the package. To break the inner vial, crush ONCE between the thumb and forefinger at the dot located at the center of the inhalant. Pass the inhalant back and forth close to the nose of the affected person several times. If the condition persists, consult a physician. Discard inhalant after use. Caution-Ammonia Inhalant formulation is flammable. Keep away from heat and open flame.
James Alexander’s Ammonia Inhalants are offered as a unit dose inhalant containing 0.3 mls of solution in the following packaging options:
Safety Data Sheet | Pricing | Drug Facts
Povidone iodine topical solution USP (PVP) is an aqueous formulation of povidone-iodine, a compound formed by heating 1-vinyl-2-pyrrolidinone with elemental iodine. The povidone component serves the function of iodide in aqueous iodine solutions and tinctures, which is to increase the solubility and to provide a slow release form of iodine.
As compared to iodine solutions and tinctures, PVP solutions offer the following advantages:
PVP Topical solutions retain the broad spectrum antimicrobial and antiviral activity of iodine. It is used for the prevention of infection in minor burns, abrasions and cuts and in the preparation of the skin for injection and hyperalimentation procedures.
James Alexander’s Povidone iodine USP swabs carry a five (5) year expiration date, the maximum amount allowed by the Food and Drug Administration.
Reverse cardboard sleeve on swab. Crush ONCE between the thumb and forefinger at the dot located at the center of the swab. Gently squeeze swab to apply to the desired area. To avoid glass splinters, use only with paper cap completely in place.
James Alexander offers PVP Topical Solution USP as a 10% solution packaged in unit dose swab containing 0.6 mls of solution.
Medicaine® Sting and Bite Relief is a James Alexander Corporation proprietary formulation that provides relief of pain and itching associated with insect bites and stings.
Medicaine® Sting and Bite Relief was developed in accordance with the Food and Drug Administration’s proposed rules for over-the counter topical analgesic drug products and contains two active ingredients (menthol and benzocaine) in the maximum allowable concentrations:
James Alexander has combined these two highly effective active ingredients in a water soluble base that assures the formulation’s effectiveness.
James Alexander’s Medicaine® Sting and Bite Relief Formulation swabs carry a five (5) year expiration date, the maximum allowed by the Food and Drug Administration.
Reverse cardboard sleeve on swab. Crush ONCE between the thumb and forefinger at the dot located at the center of the swab. Gently squeeze swab to apply to the desired area. To avoid glass splinters, use only with paper cap completely in place. Caution: Do not use in the eyes. Not for prolonged use. If the pain or itching associated with the bite or sting persists or if swelling develops, discontinue use and consult a physician.
James Alexander offers Medicaine® Sting and Bite Relief Formulation as a unit dose swab containing 0.6 mls of solution.
Safety Data Sheet | Pricing | Drug Facts
For smaller order quantities, please contact Caligor Rx
Caligor Rx Inc.
(212)-988-1729
inquiries@caligorpharmacy.com