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AEMCOLO is for the treatment of adults with travelers' irritable bowel (TD) caused by E.coli. It is the first FDA-approved antibiotic in a decade for the treatment of TD—designed to stay in your colon to help fight the infection at its source.

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse sem ligula, luctus at rutrum ac, dignissim eu risus. Etiam tincidunt mattis neque, eget interdum sapien imperdiet quis. Aliquam at sapien a dolor blandit consectetur. Pellentesque est nulla, feugiat eu pellentesque quis, consectetur vel odio. Donec placerat justo eget venenatis hendrerit. Mauris a ex vitae leo rhoncus molestie. Vivamus a mollis massa. Duis elementum tempus posuere. Nunc tincidunt lectus at nisl egestas, a tincidunt nisi condimentum. Nam egestas, nunc vitae vulputate malesuada, dolor lectus rhoncus tortor, a aliquet tellus dui sit amet massa. Vivamus sed sapien vel libero lacinia rutrum. Suspendisse potenti. Sed sit amet neque sit amet diam eleifend eleifend nec eget mauris. Aliquam id aliquet dolor, ac consectetur ipsum. Integer est mi, rhoncus id tincidunt at, efficitur et leo. Vestibulum maximus dictum orci, ac eleifend libero consectetur et. Vivamus pretium ac odio at condimentum. Donec dictum eu enim ut egestas. Nam nisi urna, elementum a eros a, scelerisque pulvinar sem. Phasellus rhoncus nisl quis eros consequat, et fermentum purus convallis. Etiam egestas nibh nec lacus accumsan porttitor. Nunc viverra mauris arcu, vitae convallis ante molestie vel. Sed fringilla neque tristique erat egestas, in venenatis tortor sodales. Proin in fermentum augue, at tristique nulla. Donec id rhoncus elit. Nam sodales est vel odio dapibus, mollis egestas orci bibendum. Ut pretium eros vel ullamcorper pretium. Praesent neque ipsum, venenatis faucibus ante sed, egestas molestie mauris. Aenean egestas erat dui, et pellentesque mauris ultricies id. Nam vitae tristique ligula. Curabitur quam diam, tempor at quam sed, malesuada congue nisi. Donec efficitur ex in nisi efficitur ullamcorper. Curabitur eget accumsan justo, ut interdum libero. Phasellus pharetra lectus lorem, quis finibus turpis rhoncus sit amet. Lorem ipsum dolor sit amet, consectetur adipiscing elit. Maecenas enim tortor, tristique id interdum vel, placerat ut elit. Mauris sit amet condimentum libero, eget gravida elit. Donec efficitur arcu tortor, vel euismod arcu bibendum sed. Sed vel nulla in ipsum cursus tempus. Duis suscipit tortor rhoncus, pulvinar sapien sit amet, bibendum purus. Cras orci diam, ornare sed dignissim a, facilisis eu ante. Quisque scelerisque lorem non mi molestie sodales. Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nam sodales quis dolor at tempor. Aenean eu erat urna. Ut malesuada lacus sed felis malesuada, at hendrerit sem dapibus. Integer feugiat eleifend dolor, at eleifend est bibendum et. Quisque consequat commodo tempor. Donec eget turpis semper, efficitur ante ut, semper orci. Nulla semper libero ac scelerisque efficitur. Cras dapibus augue non tellus finibus feugiat. Nulla condimentum quam a placerat hendrerit. Suspendisse tincidunt pharetra quam eu tristique. Ut semper dapibus ullamcorper. Nam ac placerat tellus. Nulla vel vestibulum odio, a rhoncus dolor. Maecenas venenatis consequat aliquet. Sed maximus leo eu enim rutrum fermentum. Integer at tempus ligula.

Information about AEMCOLO

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How does it work?

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Take a solid stand against TD with this FDA-approved antibiotic for unwanted bowel movements. AEMCOLO takes down noninvasive strains of E. coli with ease, giving you ultimate relief.

AEMCOLO

Aemcolo

All oral contraceptive (OC) orders will consist of 3 cycles. *Minimum order 3 cycles

Azurette (desogestrel/ethinyl estradiol and ethinyl estradiol tablets USP) is available in a blister card. Each blister card contains 28 tablets in the following order:
<ul>
<li>21 white tablets containing 0.15 mg desogestrel and 0.02 mg ethinyl estradiol</li>
<li>2 light green tablets (inert)</li>
<li>5 light blue tablets containing 0.01 mg ethinyl estradiol</li>
</ul>
<a href="https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ce13d459-3096-4899-9975-7e932260a14f&amp;audience=consumer" target="_blank" rel="noopener">Read Full Prescribing Information</a>

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Extensive catalog

azurette-3

azurette

Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol tablets

Compares to: Bekyree™, Kariva®, Mircette®, Pimtrea™, Viorele

Azurette®

Kariva®

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Finasteride is a prescription medicine used for the treatment of male pattern hair loss (androgenetic alopecia). It is not known if finasteride works for a receding hairline on either side of and above your forehead (temporal area).

Finasteride tablets, USP are for use by MEN ONLY and should NOT be used by women or children. Read this Patient Information before you start taking finasteride and each time you get a refill. There may be new information. This information does not take the place of talking with your healthcare provider about your medical condition or treatment.
&nbsp;
Finasteride is a prescription medicine used for the treatment of male pattern hair loss (androgenetic alopecia).
It is not known if finasteride works for a receding hairline on either side of and above your forehead (temporal area).

Finasteride tablets may be administered with or without meals.The recommended dose of finasteride is one tablet (1 mg) taken once daily.
In general, daily use for three months or more is necessary before benefit is observed. Continued use is recommended to sustain benefit, which should be re-evaluated periodically. Withdrawal of treatment leads to reversal of effect within 12 months.

Decrease in your blood Prostate Specific Antigen (PSA) levels.Finasteride can affect a blood test called PSA (Prostate-Specific Antigen) for the screening of prostate cancer. If you have a PSA test done you should tell your healthcare provider that you are taking finasteride because finasteride decreases PSA levels.
&nbsp;

Increased Risk of High-Grade Prostate Cancer with 5α-Reductase Inhibitors
Men aged 55 and over with a normal digital rectal examination and PSA ≤3.0 ng/mL at baseline taking finasteride 5 mg/day (5 times the dose of finasteride) in the 7-year Prostate Cancer Prevention Trial (PCPT) had an increased risk of Gleason score 8 to 10 prostate cancer (finasteride 1.8% vs placebo 1.1%). Similar results were observed in a 4-year placebo-controlled clinical trial with another 5α-reductase inhibitor (dutasteride) (1% dutasteride vs 0.5% placebo). 5α-reductase inhibitors may increase the risk of development of high-grade prostate cancer. Whether the effect of 5α-reductase inhibitors to reduce prostate volume, or study-related factors, impacted the results of these studies has not been established.

Finasteride is not indicated for use in pediatric patients.
&nbsp;

Information about Finasteride

If you’ve noticed your hair thinning around the top of your head or receding at the temples, there’s a good chance that you have male pattern baldness. You might also start noticing hair on your pillowcase or in the shower, but don’t worry—finasteride can help prevent and even reverse the hair loss process.

Don’t ignore the signs.

Men now have a choice whether they keep their hair, and that’s where Finasteride comes in. But it’s important to start now—it’s much harder to get your hair back once it’s gone. The earlier you start treatment, the more effective it will be, so get started with Finasteride today.

Control your hair’s destiny!

How do I take it

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A longstanding generic and one of the most commonly prescribed medications in the United States. Finasteride prevents genetic hair loss and encourages growth by blocking DHT, a testosterone-derived steroid that shrinks hair follicles.

Finasteride

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PRJKT RUBY partners with Population Services International (PSI) to expand access to affordable contraceptives globally. This collaboration taps into PSI's extensive network and expertise in public health, aiming to enhance the distribution and availability of contraceptives. Together, PRJKT RUBY and PSI are committed to addressing unmet family planning needs and improving reproductive health outcomes on a global scale.

Birth Control On A Mission

WARNING: CARDIOVASCULAR DISORDERS, PROBABLE DEMENTIA, BREAST CANCER, and ENDOMETRIAL CANCER See full prescribing information for complete boxed warning. Estrogen Plus Progestin Therapy <ul style="text-align:left"><li>The Women’s Health Initiative (WHI) estrogen plus progestin substudy reported increased risks of pulmonary embolism (PE), deep vein thrombosis (DVT), stroke, and myocardial infarction (MI).</li><li>The WHI estrogen plus progestin substudy reported increased risks of invasive breast cancer.</li><li>The WHI Memory Study (WHIMS) estrogen plus progestin ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older.</li><li>Do not use estrogen plus progestogen therapy for the prevention of cardiovascular disease or dementia.</li> </ul> Estrogen-Alone Therapy <ul style="text-align:left"> <li>There is an increased risk of endometrial cancer in a woman with a uterus who uses unopposed estrogens.</li> <li>The WHI estrogen-alone sub study reported increased risks of stroke and DVT.</li> <li>The WHI Memory Study (WHIMS) estrogen plus progestin ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older.</li> <li>Do not use estrogen-alone therapy for the prevention of cardiovascular disease or dementia.</li> </ul> <div style="text-align:left">The WHI estrogen-alone and estrogen plus progestin sub studies evaluated only daily oral conjugated estrogens (CE) [0.625 mg] and medroxyprogesterone acetate (MPA) [2.5 mg]. Therefore, the relevance of the WHI findings regarding adverse cardiovascular events, dementia, and breast cancer to lower CE and MPA doses, other routes of administration, or other estrogen-alone or estrogen plus progestogen products is not known and cannot be definitively excluded or determined.</div> Most important information you should know about BIJUVA (a combination of estrogen and progestogen): <ul style="text-align:left"> <li>Do not use estrogens with or without progestogens to prevent heart disease, heart attacks, strokes, or dementia (decline of brain function).</li> <li>Using estrogens with progestogens may increase your chances of getting heart attacks, strokes, breast cancer, or blood clots.</li> <li>Using estrogens with progestogens may increase your chance of getting dementia, based on a study of women 65 years of age and older.</li> <li>Using estrogen-alone may increase your chance of getting cancer of the uterus.</li> <li>Do not use estrogen-alone to prevent heart disease, heart attacks, strokes, or dementia (decline of brain function).</li> <li>Using estrogen-alone may increase your chances of getting strokes or blood clots.</li> <li>Using estrogen-alone may increase your chance of getting dementia, based on a study of women 65 years of age and older.</li> </ul> You and your healthcare provider should talk regularly about whether you still need treatment with BIJUVA. DO NOT USE BIJUVA IF YOU: <ul style="text-align:left"> <li>Have had your uterus (womb) removed (hysterectomy). BIJUVA contains a progestogen to decrease the chance of getting cancer of the uterus. If you do not have a uterus, you do not need a progestogen and you should not use BIJUVA.</li> <li>Have any unusual vaginal bleeding. Vaginal bleeding after menopause may be a warning sign of cancer of the uterus (womb). Your healthcare provider should check any unusual vaginal bleeding to find out the cause.</li> <li>Have been diagnosed with a bleeding disorder.</li> <li>Have or have had certain cancers. Estrogens may increase the chances of getting certain types of cancers, including cancer of the breast or uterus (womb). If you have or have had cancer, talk with your healthcare provider about whether you should use BIJUVA.</li> <li>Have or have had blood clots.</li> <li>Had a stroke or heart attack.</li> <li>Have or have had liver problems.</li> <li>Are allergic to BIJUVA or any of its ingredients.</li> </ul> WARNINGS Ask a doctor before use if you: <ul style="text-align:left"> <li>Have high levels of fat in your blood (triglycerides).</li> <li>Have any unusual vaginal bleeding.</li> <li>Have any other medical conditions that may become worse while you are using BIJUVA, such as: asthma (wheezing); diabetes; a genetic problem called porphyria; lupus; hypertension (high blood pressure); have high calcium in your blood; epilepsy (seizures); migraine; endometriosis; angioedema (swelling of face or tongue); problems with your heart, liver, thyroid or kidneys.</li> <li>Are going to have surgery or will be on bed rest.</li> <li>Are pregnant or think you may be pregnant. BIJUVA is not for pregnant women.</li> <li>Are breastfeeding.</li> </ul> Tell your doctor or pharmacist about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. WHEN USING BIJUVA, YOU MAY HAVE <ul style="text-align:left"> <li>Breast tenderness</li> <li>Headache</li> <li>Nausea</li> <li>Vaginal bleeding</li> <li>Vaginal discharge</li> <li>Pelvic pain</li> </ul> Call your doctor right away if you get any of the following warning signs: <ul style="text-align:left"> <li>New breast lumps</li> <li>Unusual vaginal bleeding</li> <li>Changes in vision or speech</li> <li>Sudden new severe headaches</li> <li>Severe pains in your chest or legs with or without shortness of breath, weakness, and fatigue</li> <li>Vomiting</li> </ul> USE <div style="text-align:left">BIJUVA is a prescription medicine that contains two hormones, an estrogen, and a progestogen. BIJUVA is used after menopause to reduce moderate to severe hot flashes in women with a uterus.</div> <div style="text-align:left">The risk information provided here is not complete. To learn more, review the BIJUVA Patient Information and talk about BIJUVA with your healthcare provider or pharmacist. The FDA-approved product labeling, including Patient Information, can be found <a href="https://dailymed.nlm.nih.gov/dailymed/fda/fdaDrugXsl.cfm?setid=bc52489a-5149-411d-9665-2c75405ad15d&type=display">here</a>.</div> <div style="text-align:left">You are encouraged to report negative side effects of prescription drugs to the FDA. Visit <a href="https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program">MedWatch</a> or call 1-800-FDA-1088. </div>

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<ul style="text-align: left"> 	<li>Single-phase continuous administration regimen</li> 	<li>21 orange tablets of levonorgestrel and ethinyl estradiol</li> 	<li>7 peach non-hormone containing tablets to help ease administration</li> 	<li>28-day tablet blister pack makes dosing easy and convenient</li> </ul><a href="https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c59652c-49a6-4eed-b557-9abd3ffac541" target="_blank" style="text-decoration-line: underline">Read Full Prescribing Information</a>

MORE INFO

chateal-r-scaled-small

Chateal-R-scaled-small

Levonorgestrel and Ethinyl Estradiol tablets, USP 0.15 mg /0.03 mg

Compares to: Portia®, Altavera®, Marlisa®, Kurvelo®, Levora®

Chateal EQ®

tarina-24-fe-box-2

Tarina-24-FE-Box

Tarina® 24 Fe

Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets, 1mg/20mcg

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Donation 100

Donation 5

Donation 50

Donation

Donation 20

Donation 10

vyleesi-image

vyleesi image

Vyleesi

Vyleesi is a prescription treatment approved by the FDA for premenopausal women with hypoactive sexual desire disorder (HSDD). This medical condition impacts over 10% of women in the US and causes ongoing low sexual desire.

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Enpresse

Enpresse®

Levonorgestrel and Ethinyl Estradiol tablets USP

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Junel-Fe-1.5_30

Junel Fe® 1.5/30

Norethindrone Acetate and Ethinyl Estradiol tablets USP and Ferrous Fumarate tablets

tarina_1_20_eq_carton-small-2

Tarina_1_20_EQ_Carton-small

Tarina Fe 1/20 EQ®

Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate

aubra-r-scaled-small

Aubra-R-scaled-small

Aubra EQ®

Levonorgestrel and Ethinyl Estradiol tablets, USP 0.1 mg /0.02 mg

lyleq-r-scaled-small

Lyleq-R-scaled-small

Lyleq®

Norethindrone tablets, USP 0.35 mg

kariva-2

Kariva

Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol

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Tri-VyLibra-Lo-R-scaled-small

Tri-VyLibra® Lo

Norgestimate and Ethinyl Estradiol Tablets USP

jasmiel-2

Jasmiel

Jasmiel®

Drosperinone and Ethinyl Estradiol Tablets, USP 3.0 mg/0.02 mg

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Cryselle-small

Cryselle®

Norgestrel and Ethinyl Estradiol Tablets, USP 0.3 mg/0.03 mg

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Afaxys-Econtra-One-Step-sized

EContra One-Step

Levonorgestrel Tablet
FDA-approved for use up to 3 days (up to 72 hours) after unprotected sex or a known birth control failure. ***Note: Be sure to select Overnight Shipping if you need this ASAP.

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mega multivatamin

Mega Multivitamin Gummies

Natural Raspberry Flavored Gluten-Free Dietary Supplement

NuvaRing®

Prescription NuvaRing is a small, flexible vaginal ring used to prevent pregnancy. You put it in for 3 weeks, take it out, then put a new one in a week later. It’s just as effective as the pill when used as directed, and you don’t have to think about taking it every day. Click &#8220;Get Started&#8221; to be redirected to GetNuvaRing.com.

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ELLA-USA-sized

Ella®

Ella® (a.k.a morning after pill) can help prevent unplanned pregnancy. Ella® works for up to five days after unprotected sex or contraceptive failure. Talk to a healthcare provider online to get a prescription fast.

cyred_eq_carton-small

Cyred_EQ_Carton-small

Cyred EQ®

Cyred EQ® Desogestrel and Ethinyl Estradiol tablets, USP, 0.15mg/0.03 mg

sprintec-dl

Sprintec®

Norgestimate and Ethinyl Estradiol tablets