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The number one reason
for visiting the doctor? You guessed
it! Pain. Pain is the most debilitating
medical symptom doctors see - chronic pain
impacts over 90 million Americans and costs
us an estimated $500 billion dollars each
year.
Traditional pain relievers and
topical formulas offer only limited relief
for back and neck pain, sports injuries, Osteoarthritis,
and other painful conditions.
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Ingredients |
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Whole
Leaf
Aloe
Vera
Concentrate,
Purified
Water,
Herbal
Extract
Blend
(Arnica,
Skullcap,
Nettle,
Kava
Kava,
Chamomile,
Green
Tea,
Willow
Bark,
Witch
Hazel),
Methylsulfonylmethane
(MSM),
SD
38
Alcohol,
Menthol,
Sodium
Chondroitin
Sulfate,
Sweet
Almond
Oil,
Glucosamine
Sulfate,
Hyaluronic
Acid,
Emu
Oil,
Vitamin
E
Acetate,
Vitamin
A
Palmitate,
Oleoresin
Capsicum,
Ginger,
Coriander
Oil,
Soy
Lecithin,
Oil
of
Peppermint,
Grape
Seed
Extract,
FD&C
Blue#1,
Annatto.
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Directions:
Apply
to
affected
area
by
massaging
the
product
in
well.
Use
every
two
hours
or
as
needed.
Warning:
For
external
use
only.
Keep
out
of
eyes
and
mucous
membranes.
Keep
out
of
reach
of
children.
Discontinue
use
if
rash
or
other
reaction
occurs.
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Emu oil provides superior penetration
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Joint
support compounds and antioxidants
promote joint health.
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Greaseless, stainless
formula with a light and pleasant
fragrance.
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Safe for long-term
use
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Over $2 billion
spent every year on painkillers -
particularly anti-inflammatories (NSAIDs).
However, there is a possible association
between these medicines and hypertension (high
blood pressure), but it is possible that they
may interfere with blood pressure regulation.
Researchers at Harvard Medical School have
just completed a major study, reported in
Archives of Internal Medicine, involving
over 80,000 participants. Those who
took NSAIDs for 22 days a month or more were
found to have an 86% increased rate of developing
hypertension.
Regular use of NSAIDs increases risk
of gastrointestinal problems.
A recent study, reported in the American
Journal of Gastroenterology, found that
people who used non-prescription NSAIDs on
a regular basis had a 20% higher incidence
of gastrointestinal (GI) side effects. Researchers
at the University of Michigan found that low-dose
aspirin, enteric-coated aspirin or buffered
aspirin did not reduce the risk of these complications.
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