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Loma Psoriasis |
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A Service of |
| Holisticonline.com |
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An Effective Remedy for
Psoriasis |
LOMALUX PSORIASIS
SPECIFICATIONS AND PROOF OF
CLAIMS
LOMALUX PSORIASIS is a medicine regulated by the Food and Drug
Administration in the U.S.A. It is labeled and registered with a National Drug Code (NDC)
number in accordance with UFDA requirements and is legal for sale in the U.S.A. as an
over-the-counter drug without a doctor's prescription required. All active ingredients are
listed in and are in conformance with the requirements for OTC distribution in the United
States.
LOMALUX PSORIASIS is packaged in an 8 fluid ounce bottle,
consisting of pharmaceutical grade, clear PET plastic with white plastic cap containing
F-217 liner and tamper evident seal in place. The ingredients listed below for LOMALUX
PSORIASIS are dissolved in purified water.
LOMALUX PSORIASIS.
NDC Number 61480-122-03, (US Patent No. 5,171,581)
PROOF OF CLAIMS
LOMALUX PSORIASIS is indicated on its label for symptomatic relief
from the scaling, flaking, redness, pain and itching of psoriasis.
Active Ingredients:
| Potassium
Bromide |
Proven for
skin eruptions, raised red patches or lesions and itching; considered a "leading
remedy in psoriasis" (1,2). |
| Nickel
Sulphate |
Niccolum and
Niccolum Sulphuricum are proven for itching skin, pain and rheumatic joint pain associated
with psoriatic arthritis (1,2). |
| Sodium
Bromide |
Proven for
the melancholy and depression that can accompany chronic disease (3). |
| Zinc Bromide |
Proven for
itching, crawling skin, chronic skin eruptions, oozing and fissuring (2). |
| Potassium
Sulphate |
Proven for
abundant scaling or desquamation of the skin and associated itching; listed for the
treatment of psoriasis (1,2). |
References
- Boericke, William, MD, Materia Medica with Repertory, 1927, ninth
edition.
- Clark, John Henry, MD A Dictionary of Practical Materia Medica, 3
Vol., 1921.
- Allen, Materia Medica (out of print)
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