Mounjaro®
Starting from £179.99/mo
Start journey Learn moreEach Mounjaro KwikPen contains four weekly doses and is designed to be used over 28 days — not 30. Once you reach the final dose, the pen is finished. If an unopened pen has sat in your fridge past its expiry date or outside its recommended storage window, it should not be used. A prescriber and the Mounjaro Patient Information Leaflet are your definitive guides here. Mounjaro (tirzepatide) is a prescription-only medicine; suitability for any change to your treatment is always a clinical decision.
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Picture it: you started your Mounjaro pen on a Monday four weeks ago. You've done three injections, one left. You open the fridge and notice the label says something that makes you wonder, has this pen been in here too long? Or perhaps you simply lost track of the date. This is a question our prescribers hear most weeks, and it's worth having the answer clearly before you're standing in the kitchen at seven in the morning wondering what to do.
Each KwikPen is designed to deliver four 0.5ml injections, one per week over 28 days. The 28-day count begins from the date of the first injection, not from when you put the pen in the fridge. The tirzepatide information page explains the full device in more detail, but the short version is this: after your fourth dose the pen is empty and should be disposed of in a sharps container. There is no fifth dose sitting in reserve.
The reason storage windows matter is that the medicine's stability has been tested and guaranteed only within defined conditions. The Mounjaro SmPC, published on the Electronic Medicines Compendium (eMC), sets out exact temperature limits and time allowances for room-temperature storage. Paraphrasing those limits here would be a disservice, they are precise and the leaflet inside your box is the document to read. If yours is lost, the eMC version is freely available.
When people ask whether Mounjaro can be used after 30 days, they're usually describing one of three situations. First, a pen that has been in the fridge since before their previous injection cycle, maybe they had a week off, or delivery arrived early. Second, a pen that spent time out of the fridge at a room temperature that might or might not have been within the permitted range. Third, a pen that is technically in date but feels like it has been around for a while.
For situation one, the expiry date on the label is the governing limit. A pen stored correctly in the fridge at 2–8°C remains usable up to that printed date, even if more than 30 days have passed since you first put it in there. The fridge date is separate from the 28-day window, which only starts ticking at first use.
For situations two and three, the answer is less clear without knowing the specifics, which is exactly why the Patient Information Leaflet and your prescriber exist. You can read about using Mounjaro after 30 days in more detail, but the principle is consistent: if there is genuine doubt about whether a pen has been stored correctly, using it anyway is not the right call. A pen that looks identical may not perform identically if the cold chain has been broken.
The NHS tirzepatide medicines page is a useful plain-English reference for storage and handling questions, and it points readers toward the leaflet for specifics, sensible advice that we'd echo.
Don't inject first and ask questions later. Contact your prescribing team. That might feel like an awkward call to make, but it's far preferable to injecting a compromised pen and experiencing unexpected effects, or wasting a dose that could have been used safely with clarification. Most queries are resolved quickly.
At nume, every repeat order goes through a fresh clinical review before dispatch, a real prescriber reads your update, not an automated system. That process exists partly for moments like this, so that if you flag a storage concern when placing your next order, someone qualified can look at the full picture. You can find more about how that works on the Mounjaro treatment page or by reading about taking Mounjaro after 30 days if your question is more specific to timing.
If your pen is definitely expired or you are confident the storage window has been exceeded, the pragmatic answer is to treat it as waste, dispose of it safely, and arrange a replacement through your prescriber. The FAQs page covers common questions about the supply process. For cost context on replacement pens, the Mounjaro price page sets out what's included in a private prescription order.
A bit of preparation removes most of the ambiguity. Note the date of your first injection on the pen itself or in your phone calendar; set a reminder for day 28. Store the pen in the body of the fridge rather than the door, where temperatures fluctuate more with opening and closing. If you know travel is coming up, talk to your prescriber in advance about timing your supply so you're not mid-pen during a hot week away.
The experiences people share about using Mounjaro past the 30-day mark are understandably varied, because the circumstances vary, a pen stored perfectly at 2–8°C for 35 days before first use is very different from one left on a warm shelf for a week. Treating each situation on its own facts, with clinical input where there is doubt, is the only sensible approach.
If your treatment plan needs reviewing alongside a storage or timing question, a free consultation through our treatment page puts you in front of a GPhC-registered prescriber the same day. It is the right starting point whenever you are unsure.
The people
Superintendent Pharmacist (GPhC No. 2217101)
Accountable for the safe running of our registered pharmacy, from every dispensing check to every dispatch.
Clinical Lead (GPhC No. 2231744)
Sets our clinical standards and checks everything we publish against current MHRA guidance.
Independent Prescriber (GPhC No. 2084501)
Personally reviews consultations and assesses whether treatment is clinically appropriate, and leads dose adjustments and follow-up checks.
Independent Prescriber (GPhC No. 2083426)
Personally reviews consultations and assesses whether treatment is clinically appropriate, and leads dose adjustments and follow-up checks.