Sample Page - BTW Solutions

This is an example page. It’s different from a blog post because it will stay in one place and will show up in your site navigation (in most themes). Most people start with an About page that introduces them to potential site visitors. It might say something like this:

Hi there! I’m a bike messenger by day, aspiring actor by night, and this is my website. I live in Los Angeles, have a great dog named Jack, and I like piña coladas. (And gettin’ caught in the rain.)

…or something like this:

The XYZ Doohickey Company was founded in 1971, and has been providing quality doohickeys to the public ever since. Located in Gotham City, XYZ employs over 2,000 people and does all kinds of awesome things for the Gotham community.

As a new WordPress user, you should go to your dashboard to delete this page and create new pages for your content. Have fun!

VIVA Patch
SOOTHING TOPICAL PAIN RELIEF PATCH

Three Active Ingredients Combine To Not Only Fight Pain, But Also Attack Inflammation. VIVA Patch Features An Anti-Inflammatory – Providing You Hours of Relief.

VIVA Patch is a topical pain relief patch with Lidocaine, Camphor, and Methyl Salicylate (NSAID) that provides soothing pain and inflammation relief. Formulated without an overbearing scent.

Medical grade adhesive is included with each 15-count unit box.
Active Ingredients: Lidocaine 2.5%, Methyl Salicylate 4%, Camphor 2% Precautions

Patients should use no more than two patches per day

Dispose of any patch from a pouch that has been opened for 7 or more days

Safely discard used patches by folding the adhesive together.

Discard away from small children and pets

Applications

Clean and dry the affected area

Open pouch and remove one patch

Remove protective film from the medicated patch

Carefully apply patch to the affected area of pain and leave in place for up to 12 hours

If pain lasts after using the first patch, a second patch may be applied for up to another 12 hours

Only use one patch at a time

Wash hands after applying or removing patch

Reseal pouch containing unused patches after each use

Use Only As Directed by Your Physician
Details Quick View
THE RECOVERY SHOP™
The Recovery Shop provides patients direct access and convenience to the key products their physician recommends in assisting them in their recovery. These are products not covered by insurance.

Unique E-commerce portal for each practice/physician

Secure transaction functionality via CC/HSA

Customized product offering per physician recommendation

Direct delivery to the patient’s home

No implementation costs or investment

Ancillary revenue to the practice

Decreased burden on staff

A revenue generating, physician driven, patient specific e-commerce website for the purchase of post-op recovery items. Why The Recovery Shop?
The Recovery Shop was born out of an idea that patients need somewhere to purchases products that are not covered by their insurance. Insurances are covering less and less of everything! These products used to be easy to get at your local mom and pop store/pharmacy. Those days are gone. People are directed to large online retailers where there are hundreds of options to choose from. This causes confusion for the patient and increases questions that have tobe answered by the doctorsstaff. PlusCVS and Amazon are making all ofthe money. We thought there has tobe a better way!
Who Is The Recovery Shop For?

ANY Individual Doctor, Physician Group, Hospital or Surgery Center

Anyone referring patients to buy products off Amazon

Anyone using a Joint Program Coordinator/Navigator

How It Works

We create an E-Commerce website for each physician, group, hospital or surgery center

Each individual doctor has the ability toselect products that they would prefer their patients to buy and use for post-op recovery

Selections are made by body part and/or surgical procedure

Patients only see what the physicians want them to see

Products are Cash Pay/HSA Pay Only –We do not accept Insurance (these products are not covered by insurances)

The Patient Process
Upon booking surgery, the patient is provided with an instruction sheet (via email or pre-op packet) which directs patients to the website.

Patients select their group/hospital/center

Patients select their physician

Patients select their body part/surgical procedure

Patients see “Products Recommended by your Physician”

Patients choose which products they would like to purchase and put in their credit card (like any other e-commerce website)

Patients receive a confirmation email and products are delivered to their house (via FedEx/UPS) in 1-5 business days

The Products
This is your webpage. We can Sell anything you think is appropriate to help patients with their recovery.
Some of the Products:

Cold Therapy Machines (NICE, BREG, OSSUR)

Aids to Daily Living (ADLS)

Bathroom Safety Items (Raised toilet seat, shower chair etc.)

Scar Cream

Recovery Items –Massage Gun, Foam Rollers

Compression Socks

DVT Units

Nutrition Supplements
Details Quick View
Squid Sequential Compression with Cold Therapy Wraps

Squid operates by combining sequential compression with cold therapy. Each Squid wrap was uniquely developed for a specific body part with a sequential compression bladder* designed to direct swelling away from the treated body part while driving cold deep into the tissue. The combination of directional sequential compression and deep penetrating cold may help in reducing edema and pain while allowing better blood circulation in the treated area and reducing inflammation. For athletes Squid is an excellent recovery tool providing high efficacy cold therapy while driving metabolites such as lactic acid away from the treated muscle, increasing local circulation and getting you ready faster for more action! The sequential compression and cold work together to remove lactic acid and drive the cold deep into the treated muscle or joint. MUSCLE & JOINT RELIEF
Squid is designed to provide tremendous relief from muscle and joint pain.
This may allow users to reduce dependency on pain medication, perform everyday tasks that were previously painful, and enjoy walking, running, skiing, playing tennis, golf and other sports again. INJURY RECOVERY
Squid revolutionizes injury recovery by combining sequential intermittent compression with cold treatment to provide maximum results.
Squid drives the cold treatment deep into the tissue, reducing swelling and directing fluids away from the treated area towards the heart. Swelling is reduced, thereby improving blood flow to the injured tissue and delivering much needed nutrients and oxygen. PERFORMANCE RECOVERY
Squid's patent pending sequential intermittent compression assists many world-class athletes in post-workout and post-performance recovery.
Squid can be used in many ways: from elbow wraps for tendonitis, to shoulder wraps for pitchers, to leg wraps for runners and soccer players. Squid is designed to speed up performance recovery by helping remove lactic acid and other metabolites from muscles.

Details Quick View
SpinalStim
Increase Success Rates in Spinal Fusion

The SpinalStim™ device provides a safe and effective non-surgical treatment to improve fusion healing. The device uses a pulsed electromagnetic field (PEMF) to induce a low-level electrical field at the fusion site which stimulates bone healing.2-4

The only bone growth stimulation therapy device approved by the FDA as both a lumbar spinal fusion adjunct and as a non-surgical treatment for spinal pseudarthrosis.2-4

92% overall clinical success rate for adjunctive, consistent users. 2-3

Improves success rates in spinal fusions by 36% 2,3

360 degrees of pulsed electromagnetic field (PEMF) treatment around the fusion site that evenly penetrates across tissue, bone and fixation5,6

PEMF coverage up to 5 vertebral levels5

NASS coverage recommendations support the use of PEMF stimulation as an adjunct to spinal fusion surgery in high-risk patients7

Adjunctive PEMF treatment can be recommended for patients who are at high risk for pseudarthrosis8

Brief Prescribing Information:

The SpinalStim™ device is indicated as a spinal fusion adjunct to increase the probability of fusion success and as a nonoperative treatment of salvage of failed spinal fusion, where a minimum of nine months has elapsed since the last surgery. Cardiac pacemakers may be adversely affected by exposure to pulsed electromagnetic fields. Use of this device is contraindicated where the individual has an implanted cardiac pacemaker.

Full prescribing information can be found in product labeling on our patient education website BoneGrowthTherapy.com or by calling Patient Services at 1-800-535-4492.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.

References: 1. iData Research Inc., U.S. Market for Spinal Implants and VCF (iDATA_USSP19_RPT), iData Research Inc (www.idataresearch.net) 2017. 2. PMA P850007/S6. February 1990. 3. Mooney V. Pulsed electromagnetic fields: an adjunct to interbody spinal fusion surgery in the high risk patient. Surg Technol Int 1993, 2:405-410. 4. Simmons JW Jr, Mooney V, Thacker I. Pseudarthrosis after lumbar spine fusion: nonoperative salvage with pulsed electro-magnetic fields. Am J Orthop. 2004;33(1):27-30. 5. Zborowski M, Androjna C, Waldorff EI, Midura RJ. Comparison of therapeutic magnetic stimulation with electric stimulation of spinal column vertebrae. IEEE Transactions on Magnetics, Vol. 51, No. 12, December 2105, 5001009. Erratum in IEEE Transactions on Magnetics, Vol. 53, No. 2, February 2017, 9700101. 6. Navarro, M., Michiardi, A., Castano, O., & Planell, J.. (2008). Biomaterials in ortho-paedics. Journal of the Royal Society Interface, 5(27), 1137-1158. 7. Spine.org. 8. Ethan Cottrill, MS, Zach Pennington, BS, A. Karim Ahmed, BS, Daniel Lubelski, MD, Matthew L. Goodwin, MD, PhD, Alexander Perdomo-Pantoja, MD, Erick M. Westbroek, MD, Nicholas Theodore, MD, Timothy Witham, MD, and Daniel Sciubba, MD Department of Neurosurgery, The Johns Hopkins School of Medicine, Baltimore, Maryland The effect of electrical stimulation therapies on spinal fusion: a cross-disciplinary systematic review and meta-analysis of the preclinical and clinical data SOURCE: J Neurosurg Spine, October 8, 2019.
Contact Us Details Quick View
samSport Kit
Developed and clinically proven to reduce chronic joint pain and accelerate soft tissue healing, sam® is the only FDA cleared long duration home use ultrasound device.

The sam® wearable long duration continuous ultrasound device was developed by millions of dollars of government healthcare funding to reduce surgery and treat chronic pain. i. Link: https://samrecover.com/clinical-evidence/ ii. Link: https://www.nimhd.nih.gov/news-events/features/clinical-health-services/wearable-ultrasound.html

The wearable ultrasonic soft-tissue healing and pain management device is recommended and used by tens of thousands of elite athletes, injured workers and military personnel i. Link: https://samrecover.com/testimonials/

Joint Arthritis Pain Treatment with sam®: In a clinical research study on sam® long duration continuous ultrasound treatment for knee osteoarthritis, patients experienced a 52% pain reduction and 20% improvement in joint function, which were statistically significant (p<0.05). (Langer, 2014). In another placebo-controlled study on arthritis pain, sam® long duration continuous ultrasound treatment reduced joint pain by 2.5 points (48%) over six weeks of treatment which was statistically significant over the placebo 1.23 point decrease (p<0.03). (Langer, 2015). In a third double-blind placebo controlled clinical study on sam® for joint arthritis pain, patients had significant 1.96 point (40%) pain reduction for active (p<0.0001) vs. 0.85 point reduction for placebo treatment (p<0.13). Active sam® treatment patients also had significant improvement in pain, stiffness and function on the Western Ontario and McMaster Universities (WOMAC) scale compared with placebo (500 vs. 311 respectively, p<0.02). Rotational strength of the treated knee was increased by 3.2N, p=0.03) in the active treatment group. (Draper, 2018). A recent 2019 systematic review and meta-analysis on therapeutic ultrasound diathermy for knee osteoarthritis included 15 studies. The results demonstrated that therapeutic ultrasound significantly relieved pain (p<0.00001) and reduced the Western Ontario and McMaster Universities (WOMAC) physical function score (p=0.03). In addition, therapeutic ultrasound increased the active range of motion (p<0.00001) and reduced the Lequesne index (p<0.00001). The authors concluded that therapeutic ultrasound is a safe treatment to relieve pain and improve physical function in patients with knee osteoarthritis. (Wu, 2019). Langer MD, Levine V, Taggart R, Lewis GK, Hernandez L, Ortiz R. Pilot Clinical Studies of Long Duration, Low Intensity Therapeutic Ultrasound for Osteoarthritis. Proc IEEE Annu Northeast Bioeng Conf. 2014 Apr;2014:14789673. doi: 10.1109/NEBEC.2014.6972850. PMID: 25788823; PMCID: PMC4361017. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361017/ Langer MD, Lewis GK Jr. Sustained Acoustic Medicine: A Novel Long Duration Approach to Biomodulation Utilizing Low Intensity Therapeutic Ultrasound. Proc SPIE Int Soc Opt Eng. 2015 May;9467:94670I. doi: 10.1117/12.2178213. PMID: 30078928; PMCID: PMC6070146. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070146/ Draper DO, Klyve D, Ortiz R, Best TM. Effect of low-intensity long-duration ultrasound on the symptomatic relief of knee osteoarthritis: a randomized, placebo-controlled double-blind study. J Orthop Surg Res. 2018 Oct 16;13(1):257. doi: 10.1186/s13018-018-0965-0. PMID: 30326947; PMCID: PMC6192104. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192104/ Wu Y, Zhu S, Lv Z, Kan S, Wu Q, Song W, Ning G, Feng S. Effects of therapeutic ultrasound for knee osteoarthritis: a systematic review and meta-analysis. Clinical rehabilitation. 2019 Dec;33(12):1863-75. https://www.ncbi.nlm.nih.gov/pubmed/31382781 Upper Back, Neck and Shoulder Pain Treatment with sam®: A double-blind placebo controlled clinical trial of a self-applied sam® long duration ultrasound device was compared to placebo for trapezius myofascial pain over 10 treatment sessions. Active sam® treatment demonstrated a significant 190% reduction in pain and 158% improvement in health compared to placebo after only 1-hour of treatment (p<0.05) (Lewis, 2013). An additional double-blind placebo controlled study on sam® for trapezius myofascial pain was completed. Patients treated with active therapy observed a significant mean pain reduction from baseline of 2.61-points for active (p<0.001), compared to 1.58-points reduction from baseline for placebo (p=0.087), resulting in a significant 1.03-point greater decrease in active over placebo (p=0.003). Overall health quality score was significantly higher in the active group at 2.84 points compared to the placebo group at 0.46 points (p<0.001). (Patterson, 2020). Two recent 60 and 54 subject placebo-controlled studies on therapeutic ultrasound diathermy for trapezius myofascial pain demonstrated significant reduction in pain for active continuous ultrasound, respectively. The authors concluded that therapeutic ultrasound is an effective treatment of myofascial pain syndrome, and continuous therapy is the most effective. (Ilter, 2015), (Yildirim, 2018). A systematic review and meta-analysis (1966-2016) on therapeutic ultrasound including 10 studies and 428 subjects demonstrated that therapeutic ultrasound significantly reduced pain intensity and increased pain threshold. (Xia, 2017).
Lewis Jr GK, Langer MD, Henderson Jr CR, Ortiz R. Design and evaluation of a wearable self-applied therapeutic ultrasound device for chronic myofascial pain. Ultrasound in medicine & biology. 2013 Aug;39(8):1429. https://www.ncbi.nlm.nih.gov/pubmed/23743101

Petterson S, Plancher K, Klyve D, Draper D, Ortiz R. Low-Intensity Continuous Ultrasound for the symptomatic treatment of upper should and neck pain: A randomized, double-blind placebo-controlled clinical trial. Journal of Pain Research, Accepted 2020.

Ilter L, Dilek B, Batmaz I, Ulu MA, Sariyildiz MA, Nas K, Cevik R. Efficacy of pulsed and continuous therapeutic ultrasound in myofascial pain syndrome: a randomized controlled study. American journal of physical medicine & rehabilitation. 2015 Jul 1;94(7):547-54.

https://www.ncbi.nlm.nih.gov/pubmed/25299534

Yildirim MA, Öneş K, Gökşenoğlu G. Effectiveness of Ultrasound Therapy on Myofascial Pain Syndrome of the Upper Trapezius: Randomized, Single-Blind, Placebo-Controlled Study. Arch Rheumatol. 2018 Mar 23;33(4):418-423. doi: 10.5606/ArchRheumatol.2018.6538. PMID: 30874250; PMCID: PMC6409164

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409164/

Xia P, Wang X, Lin Q, Cheng K, Li X. Effectiveness of ultrasound therapy for myofascial pain syndrome: a systematic review and meta-analysis. J Pain Res. 2017 Mar 7;10:545-555. doi: 10.2147/JPR.S131482. PMID: 28331357; PMCID: PMC5349701.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349701/
Details Quick View
PhysioStim
Healing Success in Common Nonunion Fractures

PhysioStim™ devices provide a safe and effective non-surgical treatment to improve nonunion fracture healing. These devices use a pulsed electromagnetic field (PEMF) signal to induce a low-level electrical field at the fracture site which stimulates bone healing. 2,3

Proven Effective Therapy

Anatomically Designed Models

360 degrees of PEMF treatment around the fracture site that evenly penetrates across tissue, bone and fixation1,7

Single-piece, cordless design that allows for ease of placement and patient mobility

Commitment to Outcomes

PhysioStim devices are accompanied by the STIM onTrack™ mobile app, which provides patients with a treatment calendar, therapy reminder, outcome measurement tools and additional educational resources.

STIM onTrack mobile app combined with the Orthofix DIRECT™ Physician Portal enables physicians to remotely:

View patient adherence to prescribed treatments

View patient reported outcome measures (PROM) questionnaire responses

Manage new and submitted patient prescriptions

Brief Prescribing Information:

The PhysioStim™ device is indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, where the width of the nonunion defect is less than one-half the width of the bone to be treated. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.

Use of this device is contraindicated where the individual has synovial pseudarthrosis. Demand type pacemaker operation may be adversely affected by exposure to pulsed electromagnetic fields. The safety and effectiveness of this device has not been established for individuals lacking skeletal maturity or individuals with a nonunion secondary to, or in connection with, a pathological condition. The safety of this device for use on patients who are pregnant or nursing has not been established. Rare instances of reversible minor discomfort have been reported.

Full prescribing information can be found in product labeling on our patient education website BoneGrowthTherapy.com or by calling Patient Services at 1-800-535-4492.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.

References: 1. Data on file. Field mapping analysis conducted by M. Zborowski, Ph.D., Cleveland Clinic 2. PMA P850007. February 1986 3. Garland DE, Moses B, Salver W. Fracture healing: Long-term follow-up of fracture nonunions treated with PEMFs. Contemp Orthop. 1991;22(3):295-302 4. Orthofix patient registry. PMA P850007/S20. Data on file. 5. iData Research Inc., U.S. Market for Spinal Implants and VCF (iDATA_USSP19_RPT), iData Research Inc (www.idataresearch.net) 2017 6. iData Research Inc., U.S. Market for Orthopedic Trauma Devices (iDATA_USTRA19_RMS), iData Research Inc (www.idataresearch.net) 2019 7. Navarro, M., Michiardi, A., Castano, O., & Planell, J.. (2008). Biomaterials in orthopaedics. Journal of the Royal Society Interface, 5(27), 1137-1158
Details Quick View
OrthoCor Wrist Brace
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.

Drug-free pain relief

Wearable design for therapy on the go

Noninvasive and easy-to-use

Helps return your patient to an active lifestyle
Details Quick View
OrthoCor Back Brace
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.

Drug-free pain relief

Wearable design for therapy on the go

Noninvasive and easy-to-use

Helps return your patient to an active lifestyle
Details Quick View
OrthoCor Ankle Brace
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.

Drug-free pain relief

Wearable design for therapy on the go

Noninvasive and easy-to-use

Helps return your patient to an active lifestyle
Details Quick View
NICE Cold + Compression Therapy System
The NICE1 uses advanced technology to greatly improve the convenience and efficacy of cold + compression therapy without ice.
It also provides programmable pneumatic compression which is proven to reduce edema and speed recovery. NICE1 integrates these highly effective therapies in a small (8 x 8 x 8 inches) and lightweight (9 lbs.) package with an easy-to-use touch screen interface.

NO ICE - NICE1 is an iceless system. This is a clear point of differentiation when compared with other cold therapy devices.

SMALLER & LIGHTER - NICE1 is the smallest and lightest cold + compression therapy device on the market.

SIMPLICITY - NICE1 has an extremely intuitive graphical touch screen interface that makes it easy to operate.

DESIGN-FORWARD - NICE1 is focused on a superior user experience, blending pro-tested design with state-of-the-art technology.

NICE1 is a breakthrough product in the sports medicine market, a market that increasingly relies on both technology and design. We’ve worked with top surgeons, engineers and industrial designers to create a superior product. Cooling State-of-the-art technology delivers therapeutic cooling without ice. The most convenient way to apply cold therapy. Compression Programmable intermittent and constant compression greatly improves the effectiveness of cold therapy and promotes healing. Recovery By combining the therapeutic benefits of cooling and compression in a single easy-to-use device, recovery times are greatly improved.
Contact Us To Purchase Details Quick View
Manamed PlasmaFlow™
The PlasmaFlow™ is intended to be an easy-to-use sequential compression system prescribed by a physician, for use in the home or clinical setting to help prevent the onset of DVT in patients by stimulating blood flow in the extremities by simulating muscle contractions. This device is used to aid in preventing DVT by enhancing blood circulation, diminishing post-operative pain and swelling, and enhancing wound healing. Features:

Long-lasting rechargeable battery. Up to 10 hours of use on one charge

2 Modes: Continuous inflation and Step-Up inflation technology which allows the unit to increase pressure in slower increments to 55mmHG

2 LCD screens to monitor usage and pressure

Portable, lightweight, and tubeless
Details Quick View
Lidopro® Topical Pain Relief Ointment
Prescription-Strength Pain Relief Available Over-The-Counter

The Only Formulation of Its Kind – An Anesthetic, Anti-Inflammatory, Analgesic, and Counterirritant Combine with Two Skin Conditioners

to Provide Patients with Powerful Relief from Pain and Inflammation.

LidoPro^®Ointment – Topical Pain Relief Ointment

A safe and effective pain relief ointment to help treat and manage your pain. LidoPro^®contains 4 active ingredients that provide anti-inflammatory (NSAID), analgesic, and anesthetic properties to address both acute and chronic pain symptoms. Built with a hands-free applicator for easy application.

Designed to relieve muscle pain, joint pain, and injuries associated with backache, neckache, soreness, sprains, stiffness, or strains.

Active Ingredients Purpose

Lidocaine 4% - Topical Anesthetic

Menthol 10% - Topical Analgesic

Capsaicin 0.0325% - Counterirritant

Methyl Salicylate 27.5% - Nonsteroidal Anti-Inflammatory Drug (NSAID)

Inactive Ingredients:

Allantoin, Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cetyl Alcohol, Chamomilla Recutita Matricaria Flower Extract, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Inulin Lauryl Carbamate, PEG-100 Stearate, Phenoxyethanol, Stearic Acid, Triethanolamine, Water.

Directions

Adults 18 Years and Older:

Clean and dry the affected area

Apply product directly to your skin, up to 4 times daily

Wash hands after use with warm, soapy water for 30-45 seconds

Other Information

Store in a cool, dry place with lid tightly closed

Do Not Use:

If allergic to any NSAIDS

On damaged or irritated skin

With a bandage or heating pad

Other than as directed

When Using This Product: Avoid Contact With Eyes. Stop Use and Ask a Doctor if:

Condition worsens

Excessive skin irritation develops

Symptoms persist for more than 7 days, or symptoms clear up and occur again within 3 days

Use Only As Directed by Your Physician
Details Quick View