- Join Allē Today to Start Sharing and Earning
Rewards
- Refer a Friend by Allē Lets Consumers Earn up to
$50 to Use Towards Allergan
Aesthetics Products and Treatments
IRVINE,
Calif., June 4, 2024 /PRNewswire/ -- Allergan
Aesthetics, an AbbVie company (NYSE: ABBV), today announced
the debut of Refer a Friend, a new offering from Allē, the Allergan
Aesthetics Loyalty Rewards Program. Now, Allē Members can invite
their friends and family to join and both parties can receive
savings on Allergan Aesthetics products or treatments from brands
like BOTOX® Cosmetic (onabotulinumtoxinA), the
JUVÉDERM® Collection of Fillers, SKINVIVE by
JUVÉDERM®, CoolSculpting®,
SkinMedica®, and DiamondGlow®.
"When you are thinking about trying something new in aesthetics,
or in any market, you ask your friends and family for advice.
Market research shows that 92% of consumers trust referrals
from friends and family over other forms of
advertising1," said Jasson
Gilmore, Senior Vice President, U.S. Aesthetics. "And 86% of
Allē Members report being extremely likely or very likely to
recommend Allē to family and friends2. Whether you are
new to Allē, or you've been using it for a long time, we welcome
you to Refer a Friend and we reward you for your referral."
How It Works:
- Refer Your Friends: Current Allē Members can refer
up to five net new users per offer period with a unique referral
code.
- Friends New to Allē Receive Up to $50: Once a new user creates an Allē account
with a referral code, they will get $50 off in Allē to use on their first Allergan
Aesthetics product or treatment.
- Earn Up to $50 in Savings Per
Offer Period: With the new user's consent, the referring friend
will receive a $10 offer deposited
into their account following the new user's first transaction. Allē
Members can give $50 and earn up to
$50 for referring up to five friends,
while supplies last*. Members can view the Refer a Friend page in
their Allē app for full program details.
"When it comes to selecting an aesthetic provider, we know
consumers have a lot of choices. We also know that word of mouth
referrals are a significant driver for new patients and are
essential to growing our practice," said Shawna Chrisman, NP, founder of Destination
Aesthetics™, Inc. "With the new Refer a Friend capability from
Allē, it is even easier to harness the power of referrals and
establish relationships with new patients, no matter where they may
be on their aesthetic journey."
In serving more than seven million Members across 27,000
practices to-date, part of Allē's mission is to help educate
consumers about aesthetic treatments. Allē is the first and only
loyalty program in the aesthetics market to also offer consumers
the ability to earn points on over 50 non-Allergan Aesthetics
treatments and brands. By providing Members with information,
tools, and incentives, Allē empowers consumers along their
treatment journey, making the next product purchase or treatment
closer within reach.
For consumers interested in participating, please
visit www.alle.com to join and start taking advantage of
exclusive offers and access. For providers looking to engage with
Allē for Business, please contact your local Allergan Aesthetics
Business Development Manager.
*Allē Refer a Friend offer values and maximums are subject to
change.
About Allergan Aesthetics
At Allergan Aesthetics, an AbbVie company, we develop, manufacture,
and market a portfolio of leading aesthetics brands and products.
Our aesthetics portfolio includes facial injectables, body
contouring, plastics, skin care, and more. Our goal is to
consistently provide our customers with innovation, education,
exceptional service, and a commitment to excellence, all with a
personal touch. For more information,
visit www.allerganaesthetics.com.
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines
and solutions that solve serious health issues today and address
the medical challenges of tomorrow. We strive to have a remarkable
impact on people's lives across several key therapeutic areas –
immunology, oncology, neuroscience, and eye care – and products and
services in our Allergan Aesthetics portfolio. For more information
about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on
LinkedIn, Facebook, Instagram, X (formerly Twitter), and
YouTube.
BOTOX® COSMETIC IMPORTANT SAFETY INFORMATION AND
APPROVED USES
Approved Uses
BOTOX® Cosmetic is a
prescription medicine that is injected into muscles and used to
temporarily improve the look of moderate to severe forehead lines,
crow's feet lines, and frown lines between the eyebrows in
adults.
IMPORTANT SAFETY INFORMATION
BOTOX®
Cosmetic may cause serious side effects that can be life
threatening. Get medical help right away if you have any of these
problems any time (hours to weeks) after injection of
BOTOX® Cosmetic:
- Problems swallowing, speaking, or breathing, due to
weakening of associated muscles, can be severe and result in loss
of life. You are at the highest risk if these problems are
pre-existing before injection. Swallowing problems may last for
several months.
- Spread of toxin effects. The effect of botulinum
toxin may affect areas away from the injection site and cause
serious symptoms including: loss of strength and all-over muscle
weakness, double vision, blurred vision and drooping eyelids,
hoarseness or change or loss of voice, trouble saying words
clearly, loss of bladder control, trouble breathing, and trouble
swallowing.
BOTOX® Cosmetic dosing units are not the same as,
or comparable to, any other botulinum toxin product.
There has not been a confirmed serious case of spread of toxin
effect when BOTOX® Cosmetic has been used at the
recommended dose to treat frown lines, crow's feet lines, and/or
forehead lines.
BOTOX® Cosmetic may cause loss of strength or general
muscle weakness, vision problems, or dizziness within hours to
weeks of taking BOTOX® Cosmetic. If this happens, do
not drive a car, operate machinery, or do other dangerous
activities.
Serious and/or immediate allergic reactions have been
reported. They include: itching, rash, red itchy welts,
wheezing, asthma symptoms, or dizziness or feeling faint. Get
medical help right away if you are wheezing or have asthma
symptoms, or if you become dizzy or faint.
Do not receive BOTOX® Cosmetic if
you: are allergic to any of the ingredients in
BOTOX® Cosmetic (see Medication Guide for ingredients);
had an allergic reaction to any other botulinum toxin product such
as Myobloc® (rimabotulinumtoxinB),
Dysport® (abobotulinumtoxinA), or
Xeomin® (incobotulinumtoxinA); have a skin
infection at the planned injection site.
Tell your doctor about all your muscle or nerve
conditions, such as ALS or Lou
Gehrig's disease, myasthenia gravis, or Lambert-Eaton
syndrome, as you may be at increased risk of serious side effects
including difficulty swallowing and difficulty breathing from
typical doses of BOTOX® Cosmetic.
Tell your doctor about all your medical
conditions, including: plans to have surgery; had surgery
on your face; have trouble raising your eyebrows; drooping eyelids;
any other abnormal facial change; are pregnant or plan to become
pregnant (it is not known if BOTOX® Cosmetic can harm
your unborn baby); are breast-feeding or plan to (it is not known
if BOTOX® Cosmetic passes into breast milk).
Tell your doctor about all the medicines you
take, including prescription and over-the-counter
medicines, vitamins, and herbal supplements. Using
BOTOX® Cosmetic with certain other medicines may cause
serious side effects. Do not start any new medicines until you
have told your doctor that you have received BOTOX®
Cosmetic in the past.
Tell your doctor if you have received any other botulinum toxin
product in the last 4 months; have received injections of botulinum
toxin such as Myobloc®,
Dysport®, or Xeomin® in the
past (tell your doctor exactly which product you received); have
recently received an antibiotic by injection; take muscle
relaxants; take an allergy or cold medicine; take a sleep medicine;
take aspirin-like products or blood thinners.
Other side effects of BOTOX® Cosmetic
include: dry mouth; discomfort or pain at the injection
site; tiredness; headache; neck pain; and eye problems: double
vision, blurred vision, decreased eyesight, drooping eyelids and
eyebrows, swelling of your eyelids and dry eyes.
For more information refer to the Medication Guide or talk with
your doctor.
To report a side effect, please call Allergan at
1-800-678-1605.
Please see BOTOX® Cosmetic full
Product Information including Boxed Warning and
Medication Guide.
JUVÉDERM® Injectable Gel Fillers
Important Information
APPROVED USES
JUVÉDERM® VOLUX® XC injectable gel is for
deep injection to improve moderate to severe loss of jawline
definition in adults over the age of 21.
JUVÉDERM® VOLUMA® XC injectable gel is for
deep injection in the cheek area to correct age-related volume loss
and for augmentation of the chin region to improve the chin profile
in adults over 21.
JUVÉDERM® VOLLURE® XC,
JUVÉDERM® Ultra Plus XC, and JUVÉDERM® Ultra
XC injectable gels are for injection into the facial tissue for the
correction of moderate to severe facial wrinkles and folds, such as
nasolabial folds. JUVÉDERM® VOLLURE® XC
injectable gel is for adults over 21.
JUVÉDERM® Ultra XC injectable gel is also for
injection into the lips and perioral area for lip augmentation in
adults over 21.
JUVÉDERM® VOLBELLA® XC injectable gel is
for injection into the lips for lip augmentation and correction of
perioral lines, and for injection into the undereye hollows to
improve the appearance of undereye hollows in adults over the age
of 21.
IMPORTANT SAFETY INFORMATION
Are there any reasons why I should not receive any
JUVÉDERM® formulation?
Do not use these
products if you have a history of multiple severe allergies or
severe allergic reactions (anaphylaxis), if you are allergic to
lidocaine or the Gram-positive bacterial proteins used in these
products, or if you have had previous allergic reactions to
hyaluronic acid fillers.
What warnings should my doctor advise me about?
- One of the risks with using dermal fillers is the unintentional
injection into a blood vessel. The chances of this happening are
very small, but if it does happen, the complications can be serious
and may be permanent. These complications, which have been reported
for facial injections, can include vision abnormalities, blindness,
stroke, temporary scabs, or permanent scarring of the skin. Most of
these events are irreversible.
- If you have changes in your vision, signs of a stroke
(including sudden difficulty speaking, numbness or weakness in your
face, arms or legs, difficulty walking, face drooping, severe
headache, dizziness, or confusion), white appearance of the skin,
or unusual pain during or shortly after treatment, you should
notify your health care practitioner immediately.
- The use of dermal fillers where skin sores, pimples, rashes,
hives, cysts, or infections are present should be postponed, as
this may delay healing or make skin problems worse.
- The effectiveness of removal of any dermal filler has not been
studied.
What precautions should my doctor advise me about?
- JUVÉDERM® VOLBELLA® XC should only be
injected into undereye hollows by doctors who have completed the
necessary training for this treatment area. To find a doctor, visit
Juvederm.com/find-a-specialist. Doctors who complete the training
will be listed with a symbol
- The safety of these products for use during pregnancy or
while breastfeeding has not been studied
- The safety of JUVÉDERM® VOLUMA® XC
has not been studied in patients under 35 years or over 65 years
for cheek augmentation, under 22 years or over 80 years for chin
augmentation.
- The safety of JUVÉDERM® VOLUX® XC,
JUVÉDERM® VOLLURE® XC and
JUVÉDERM® VOLBELLA® XC has not been studied
in patients under 22 years, and the safety of JUVÉDERM®
Ultra Plus XC and JUVÉDERM® Ultra XC has not been
studied in patients under 18 years
- The safety and effectiveness of treatment with
JUVÉDERM® products in anatomical regions outside of
their approved uses have not been established in clinical
studies
- If you have a history of excessive scarring (thick, hard scars)
or pigmentation disorders, treatment in these patients has not been
studied and may result in additional scars or changes in
pigmentation
- If you are planning other procedures including laser treatments
or a chemical peel, there is a possible risk of inflammation at the
treatment site if these procedures are performed closely before or
after JUVÉDERM® injectable gel treatment
- Tell your doctor if you are on therapy used to reduce your
body's natural defense system (such as steroids, chemotherapy, and
medicines to treat autoimmune diseases, HIV, and AIDs), as these
may increase your risk of infection; and medications that can
prolong bleeding (such as aspirin, ibuprofen, or other blood
thinners), as these may result in increased bruising or bleeding at
the injection site.
- Avoid applying makeup for 12 hours after treatment and minimize
strenuous exercise, exposure to extensive sun or heat, and
alcoholic beverages within the first 24 hours following treatment,
as these may cause temporary redness, swelling, and/or itching at
the injection site
- JUVÉDERM® VOLUMA® XC was not studied in
patients with significant loose skin of the chin, neck, or jaw
- The effect of JUVÉDERM® VOLUMA® XC
injection into the chin on facial hair growth has not been
studied
- Patients who experience skin injury near the site of
JUVÉDERM® VOLUMA® XC injection may be at a
higher risk for adverse events
- Tell your doctor if you have already been injected with dermal
fillers in the same area as the one(s) you are about to be treated
for. This information helps your doctor decide when and whether you
should get treatment
What are possible side effects of treatment?
The most
commonly reported side effects with JUVÉDERM® injectable
gels were redness, swelling, pain, tenderness, firmness,
lumps/bumps, bruising, discoloration, and itching. For
JUVÉDERM® VOLBELLA® XC, dryness was also
reported.
These side effects are consistent with other facial injection
procedures and most will resolve within 30 days. Your doctor may
choose to treat side effects persisting longer with antibiotics,
steroids, or hyaluronidase (an enzyme that breaks down hyaluronic
acid).
As with all skin injection procedures, there is a risk of
infection.
To report a side effect with any product in the
JUVÉDERM® Collection, please call the
Allergan® Product Support Department at
18773455372. Please also visit Juvederm.com or talk to your doctor
for more information.
Products in the JUVÉDERM® Collection are available
only by a licensed physician or properly licensed practitioner.
SKINVIVE by JUVÉDERM®
Injectable Gel Important Information
APPROVED USES
SKINVIVE by JUVÉDERM®
injectable gel is an injection to improve skin smoothness of the
cheeks in adults over the age of 21.
IMPORTANT SAFETY INFORMATION
Are there any reasons
why I should not receive SKINVIVE by
JUVÉDERM® treatment?
Do not use
this product if you have a history of multiple severe allergies or
severe allergic reactions (anaphylaxis), if you are allergic to
lidocaine or the Gram-positive bacterial proteins used in this
product, or if you have had previous allergic reactions to
hyaluronic acid fillers.
What Warnings should my specialist advise me about?
- One of the risks with dermal filler injection is the
unintentional injection into a blood vessel. The chances of this
happening are very small, but if it does happen, the complications
can be serious and may be permanent. These complications, which
have been reported for facial injections, can include vision
abnormalities, blindness, stroke, temporary scabs, or permanent
scarring of the skin. Most of these events are irreversible. Tell
your specialist immediately if you have changes in your vision,
signs of a stroke (including sudden difficulty speaking, numbness
or weakness in your face, arms or legs, difficulty walking, face
drooping, severe headache, dizziness, or confusion), white
appearance of the skin, or unusual pain during or shortly after
treatment
- The use of this product where skin sores, pimples, rashes,
hives, cysts, or infections are present should be postponed, as
this may delay healing or make skin problems worse
- The effectiveness of removal of any dermal filler has not been
studied
What Precautions should my specialist advise me
about?
- Minimize strenuous exercise, exposure to extensive sun or heat,
and alcoholic beverages within the first 24 hours following
treatment. Exposure to any of these may cause temporary redness,
swelling, and/or itching at the injection site
- Tell your specialist if you are using any medication that can
prolong bleeding, such as aspirin, ibuprofen, or other blood
thinners, as this may increase bruising or bleeding at the
injection site
- Tell your specialist if you are planning laser treatment,
chemical peeling, or any other procedure after SKINVIVE by
JUVÉDERM®. There is a possible risk of an inflammatory
reaction at the treatment site
- This product is intended for improving skin smoothness of the
cheeks. The safety and effectiveness for treatment in other areas
of the body have not been established
- Tell your specialist if you are on therapy used to decrease the
body's immune response, as treatment may result in an increased
risk of infection
- Tell your specialist if you are pregnant or breastfeeding. The
safety for use during pregnancy, or in women who are breastfeeding,
has not been studied
- Tell your specialist if you have a history of excessive
scarring (thick, hard scars). The safety of this product in
patients with a history of excessive scarring has not been studied
and may result in additional scars
- Tell your specialist if you have a history of pigmentation
disorders, as use of this product in patients with a history of
pigmentation disorders has not been studied and may result in
changes in pigmentation
What are the possible side effects of treatment?
The most commonly reported side effects were redness,
lumps/bumps, swelling, bruising, pain, tenderness, firmness,
discoloration and itching. Most side effects will resolve within 7
days. If they persist longer, your physician may choose to treat
them with medications, such as antibiotics, steroids, or
hyaluronidase. Additionally, there have been reports of
inflammation, nodules, unsatisfactory result, loss or lack of
improvement, allergic reaction, anxiety, blood vessel blockage,
infection, dry skin, increase or decrease in sensation, and
abscess.
Delayed-onset inflammation near the site of dermal filler
injections is one of the known adverse events associated with
dermal fillers. As with all skin injection procedures, there is a
risk of infection.
To report a side effect, please call the Allergan®
Product Support Department at 1-877-345-5372. Please also visit
SKINVIVE.com or talk to your specialist for more
information.
SKINVIVE by JUVÉDERM® is available only by a
licensed physician or properly licensed practitioner.
CoolSculpting® and CoolSculpting® Elite
Important Safety Information
CoolSculpting® and CoolSculpting® Elite are
FDA-cleared to treat visible fat bulges on the abdomen, flank,
thigh, bra fat, back fat, upper arm, and under the buttocks, chin,
and jawline. It is also FDA-cleared to affect the appearance of lax
tissue with submental area treatments. CoolSculpting®
and CoolSculpting® Elite are not a treatment for weight
loss. Some common side effects include temporary numbness,
discomfort, and swelling. Rare side effects may occur.
CoolSculpting® and CoolSculpting® Elite may
cause visible enlargement in the treated area after treatment,
which will not resolve on its own and may require surgical
intervention for correction. Ask your doctor if
CoolSculpting® or CoolSculpting® Elite is
right for you. See additional Important Safety Information at
www.coolsculpting.com.
DiamondGlow® Uses
The
DiamondGlow® device is a general dermabrasion
device that gently removes the top layer of skin and delivers
topical cosmetic serums onto the skin.
DiamondGlow® Important Safety
Information
The DiamondGlow® treatment is
not for everyone. You should not have a
DiamondGlow® treatment if you have compromised
skin quality. Tell your provider if you are pregnant or lactating,
or if you have any medical conditions, including allergies, and if
you are using topical medications on the area to be treated.
Typical side effects include a scratchy, stinging sensation
during the treatment and temporary tightness, redness or slight
swelling after the treatment. Rare serious side effects may also
occur and include severe skin irritation and allergic
reactions.
SkinMedica® Pro-Infusion Serums
Disclaimer
SkinMedica® Pro-Infusion Serums
are intended to meet the FDA's definition of a cosmetic product, an
article applied to the human body to cleanse, beautify, promote
attractiveness, and alter appearances. These products are not
intended to be drugs that diagnose, treat, cure, or prevent any
disease or condition. These products have not been approved by the
FDA and the statements have not been evaluated by the FDA.
Please talk to your provider for additional information.
SkinMedica® Important Information
Most SkinMedica® products are intended to meet the FDA's
definition of a cosmetic product, an article applied to the human
body to cleanse, beautify, promote attractiveness, and alter
appearances. These SkinMedica® products are not intended
to be drug products that diagnose, treat, cure, or prevent any
disease or condition. These products have not been approved by the
FDA and the statements have not been evaluated by the FDA.
References:
- Josh Howarth. Exploding Topics. 22+ Referral Marketing
Statistics. 2024.
https://explodingtopics.com/blog/referral-marketing-stats.
- Allergan Data on File: Allē Grow Consumer Claims Survey.
2021.
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SOURCE AbbVie