Leader in Regenerative Medicine
TM
AHEALON®
Bio-pharmaceutical Innovation
for Better Patient Outcomes
AHEALON® is a mufti-faceted
6-in-1 Prescription Medicine
for:
1. Pain mitigation
2. Inflammation reduction
3. Infection reduction
4. Stimulus for healing
5. Scar minimization
6. Wound bed moisturization
AHEALON® Prescription Only Medicine
USA FDA NDC 52793-700-02
TREATMENT CAN INCLUDE:
Burn Injuries
Radiation Dermatitis
Arthritis (including osteoarthritis
rheumatoid arthritis
psoriatic arthritis)
Rashes
Wounds (chronic/acute)
Pressure sores
Neuropathic discomfort
Any generally inflamed area.
ACTIVE INGREDIENTS in AHEALON®
consist of the following:
Arnica 10C/30C/50M
Calendula 10C/30C/50M
Echinacea ANG 10C/30C/50M
Hypericum 10C/30C/50M
Silver 10C/30C/50M
Sulfur 10C/30C/50M
Thiosinaminum 10C/30C/50M
Urtica 10C/30C/50M
These drug ingredients are listed in the Homoeopathic Pharmacopoeia of the United States (HPUS).
INACTIVE INGREDIENTS:
Sea Minerals
Potassium Sorbate
Water.
PHARMACOLOGICAL CLASS: Homeopathic drug.
AHEALON® DOSAGE FORM:
Liquid may be used Topically at 0.15 ML/spray application.
Liquid; may be used as a gauze saturant.
Liquid; may be aerosolized for bronchial/sinus use.
CLINICAL PHARMACOLOGY: The active ingredients in AHEALON® are simple biochemical compounds. The exact mechanism of action is unknown, however it is believed that AHEALON® helps to stimulate healing response mechanisms.
AHEALON® ANTI-INFLAMMATORY COMPONENTS: contribute to the following vital mechanisms of wound healing:
More Tissue Perfusion
More Oxygenation Aids
More Cellular Nutrients
More Toxin Removal
Minimize Ischemic Cascade/Necrosis
Accelerated Vascularization/Healing
Pain Reduction
All of which contribute to the stimulation of the healing response, which in turn leads to:
Accelerated Wound Closure
Less Probability of Infection
Better Patient Outcomes
More oxygenation
More toxin removal
More nutrients
AHEALON® HOW SUPPLIED: Liquid in a 2 ounce/60 ML finger-pump spray bottle made from Cobalt Blue PET for safety; sprayer has a protective over-cap; each bottle contains approximately 400 spray applications at 0.15 ML/spray.
CLINICAL STUDIES: A variety of controlled clinical studies have been favorably performed using one or more of the ingredients herein, but no study has been completed with the combination of all of the AHEALON® ingredients.
INDICATIONS: AHEALON® is indicated for the acute and chronic treatment of pain and or inflammation, as well as a general healing aid, an infection deterrent, an agent to help reduce scar tissue and a source of moisturization (dry/cracked/burned skin), that include:
All Burn Injuries
Radiation Dermatitis
Surgical Incisions
Rashes
Pruritic Conditions
Arthritis/Joint Pain
Lower Back Pain
Wounds
Pressure Sores
Tumors
Neuropathic Discomfort
Areas that are generally painful and or inflamed area.
AHEALON® SLEEP BENEFITS: Pain remediation can secondarily benefit sleep quality and duration; pain reduction can also relieve chronic stress induced Cortisol production and thus contribute to less patient stress and anxiety and the reversal of chronic non-healing wounds.
REDUCE SHOCK: Expedited use of AHEALON® as a topical spray directly onto the wounds of pain/trauma patients may quickly control pain such as to reduce the possibility of shock.
CONTRAINDICATIONS: Although there are no known contraindications, patients who are allergic to any AHEALON® ingredient should consult a physician prior to taking the medication. (Refer to Section on Hypersensitivity)
WARNING: Choking Hazard; small parts. Keep out of reach of children.
PRECAUTIONS: Topical application of AHEALON® may cause initial stinging, with progressive desensitization as treatment progresses. Carefully adjust AHEALON® dosage to those who might be hypersensitive to any of the ingredients of this drug.
HYPERSENSITIVITY: Caution should be used when administering AHEALON® to patients with a history of contact sensitivity to sulfur or silver or to the other ingredients that comprise this drug. the
INFORMATION FOR PATIENTS: Patients using AHEALON® should receive the following information and instructions:
1. AHEALON® medication is to be used throughout the healing
process only as directed by your physician.
2. It is important to systematically follow physician advised
application times; do not skip AHEALON® applications and/or
double applications.
DRUG INTERACTIONS: There are no known AHEALON® drug interactions.
CARCINOGENESIS, MUTAGENESIS, AND IMPAIRMENT OF FERTILITY: No studies have been done on the carcinogenesis, mutagenesis, or impairment of fertility of AHEALON®. In general, at the dilutions herein formulated, homeopathic drugs are not known to cause direct or indirect harm to a fetus. AHEALON® should be given to a pregnant woman only if clearly needed.
EFFECTS OF EACH INGREDIENT is not listed as a carcinogen by ACGIH, IARC, NIOSH, NTP, or OSHA; each is a GRAS substance: generally recognized as safe.
PREGNANCY CATEGORY C. Animal reproduction studies have not been conducted with AHEALON®. Pregnant women are given AHEALON® only if clearly needed.
NURSING MOTHERS: It is not known whether this drug is secreted in human milk. However, since many drugs are secreted in human milk, caution should be exercised when AHEALON® is administered to a nursing woman.
PEDIATRIC USE: Carefully adjust AHEALON® dosage when treating young children who might have a hyper-sensitivity to any of the ingredients of this drug.
ADVERSE REACTIONS: AHEALON® contains low doses of active ingredients. Therefore there are minimal known side effects. (see PRECAUTIONS for hypersensitivity information)
OVERDOSAGE: Due to the low concentrations of active AHEALON® ingredients, adverse reactions following over-dosage are extremely rare. Care must be taken not to exceed the recommended AHEALON® dosage.
DOSAGE AND ADMINISTRATION: for topical administration (each spray contains approximately 0.15 ML AHEALON®) spray 4 to 6 times, 3 to 5 inches away from: all burns, wounds, pressure sores, debrided areas, arthritis, incisions, rashes, scar tissue, painful, bruised and inflamed areas.
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For intense pain apply AHEALON® every 3 minutes, as pain subsides every 5 minutes, then every 10 minutes, adjusted for each patient, up to hourly. Pain should take longer to return after each application. Generally effective in 12 seconds to 12 minutes; results can last ¼ - 8 hours.
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Apply AHEALON® before, during and after debridement; treatment may enhance autolytic debridement.
For chronic pain/sores, spray AHEALON® as directed, such as every hour, for 2 - 6+ weeks.
For maximum absorption, AHEALON® spray should be applied to clean skin/tissue at the beginning of the day and throughout the day per physician directed regimen throughout the healing process – it is important not to miss an application.
AHEALON® For burn wounds/grafts, apply to ensure that wounds are kept in a moist condition.
AHEALON® can be used as a gauze saturant for burns/wounds.
Generally use more AHEALON® at first, then use less later.
AHEALON® Acting to stop pain/reduce inflammation allows for more tissue perfusion, which allows tissues to acquire more Oxygen and nutrients as vital growth factors for expedited wound closure and healing/infection resistance.
AHEALON® Moisturization also helps to ensure a supple wound.
AHEALON® application to nerve trunk areas, such as neck, could augment effectiveness.
Concomitant use of AHEALON® with opioid drugs may produce the same analgesic effects with less opioid use. Expedited topical use for trauma/pain patient could act to quickly stop/reduce pain and thus act to reduce the possibility of shock.
MAINTENANCE PHASE: In order to maintain symptomatic relief, AHEALON® medication should be continued at a physician advised dose level. It is important to use systematically as per physician determined regimen of times and dosage levels throughout the healing period. Treatment duration depends on each individual.
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PRODUCTS
AHEALON®
DESCRIPTION: AHEALON® is a US Patent Pending biochemical homeopathic medication indicated for the treatment of pain and or inflammation, as well as a general
healing aid, an infection deterrent, an agent to help reduce scar tissue and a source of moisturization (dry/cracked/burned skin).
Complete
description below.