Femipro Official Website › Batch verification
How To Verify A Bottle Of Femipro
This desk's current Femipro stock is lot FEM-26/FE-4936, certificate reference FEM-4936-26-FE. The lot code is printed on the base of the bottle and can be matched against your order by calling +1 (302) 200-3480. A lot code confirms which batch a bottle came from. It does not confirm what is inside it.
Five checks worth making, and a plain statement of what a batch number can and cannot tell you.
The Femipro batch record for this stock
Seven fields, and one caveat that matters more than the other six.
| Field | Value | What it means |
|---|---|---|
| Lot | FEM-26/FE-4936 | The manufacturer's batch identifier for this production run |
| Certificate of analysis reference | FEM-4936-26-FE | A reference number for a certificate held by the manufacturer. This desk does not hold the document itself |
| Form | Capsule, 30 per bottle | One capsule daily. Not a gummy, not a liquid |
| Declared actives | 350 mg + 50 mg | Two blend totals. No individual amount is published for any of the nine ingredients |
| Manufacturing | FDA-registered facility, GMP certified | Process standards under 21 CFR part 111. Neither is a test result for this batch |
| Label distributor | FemiPro, 285 Northeast Ave, Tallmadge, OH 44278, United States | The address printed on the bottle. Not this retail desk |
| Retail desk | Femipros, 75 Broad Street, Suite 2400, New York, NY 10004, USA | Who sold it to you and who handles the guarantee |
The vendor documentation this desk works from describes lot FEM-26/FE-4936 and certificate FEM-4936-26-FE as draft label references rather than laboratory proof. We are repeating that description here rather than dropping it, because it is the single most important caveat on this page.
We do not hold a certificate of analysis document. We hold a reference number for one. Those are different things, and a page that displayed a lab letter it did not possess would be committing the exact fraud this page exists to help you detect. If you need the certificate itself, the manufacturer named on the label is the party who holds it.
Five checks to make on a Femipro bottle
Five minutes, and the fifth one is the one people get wrong.
Find the lot code on the base of the bottle
This desk's current stock is lot FEM-26/FE-4936. The code and a best-before date are printed on the base when the bottle carries them.
Check the safety seal before you open it
The label instruction is explicit: “Keep out of the reach of children. Do not use if safety seal is damaged or missing. Store in a cool, dry place.” A seal that is broken, lifted or missing is a reason to stop and call the desk, not a reason to proceed carefully.
Check the count and the panel
Thirty capsules. A Supplement Facts panel naming UTI Herbal Blend at 350 mg and Probiotic Blend at 50 mg. If your panel differs from the one transcribed on our label page, your bottle is the authority and we want to hear about it.
Match the order
Call +1 (302) 200-3480 with the order ID and the lot from the base. That desk can confirm the bottle came from the stock it shipped you.
Keep the bottle until you are finished with it
Not the capsules decanted into an organiser. The lot, the expiry and the panel all live on the bottle, and every one of them is needed if a question comes up.
What a Femipro lot number cannot tell you
Five things it establishes, five it does not.
A batch code is a traceability tool. It lets a manufacturer identify which production run a bottle came from, which is what makes a recall possible. That is genuinely valuable and it is the whole of what it does.
| It does tell you | It does not tell you |
|---|---|
| Which production run the bottle came from | How much of any ingredient is in the capsule |
| That the bottle can be matched to an order this desk shipped | That the contents were tested against the label |
| That a recall could reach this bottle if one were issued | That no recall has been issued elsewhere |
| Roughly when it was made, via the best-before date | How it was stored between the factory and your door |
| That the seal was intact when it reached you | That the live cultures are still viable, since no colony count is published to check against |
The last row is the one specific to this product. A probiotic's value depends on viable organisms, no CFU figure is printed, and a lot code cannot substitute for one.
What would close that gap is a published certificate of analysis for each batch, naming the assay, the laboratory and the results. Some manufacturers do publish them. This one does not publish one to this desk, and we are not going to imply otherwise by displaying a reference number in a way that looks like a document.
The cGMP rule at 21 CFR part 111 requires manufacturers to establish identity, purity, strength and composition. That is a real obligation and it is why the GMP mark is worth more than nothing. It is an obligation on process, verified by inspection rather than by a certificate in your hand. The testing and quality page goes through every seal on this bottle on the same basis.
Every fact on our label page was transcribed from this image. If the panel on your bottle differs from it in any respect, your bottle is right and this website is out of date.
Printed FemiPro, with the capital P. Counterfeit packaging most often gives itself away in the typography and the print quality of the label rather than in the bottle, so a clean, correctly-kerned wordmark is a reasonable first check.
What a Femipro recall would actually look like
Voluntary, lot-specific, and after the fact.
A batch code only earns its place if something ever goes wrong, so it is worth knowing what that process looks like, because almost nobody explains it.
Most supplement recalls in the United States are voluntary. A manufacturer or distributor identifies a problem, often contamination or an undeclared ingredient, and withdraws the affected lots. The FDA publishes the notice and can request a recall, but under the framework described in its questions and answers on dietary supplements it has no power to approve a supplement before sale, and it acts after a product is on the market rather than before.
The lot code is the mechanism that makes any of that possible. A recall is almost always issued against specific lots rather than against a product as a whole, because the problem lives in a production run. Without the code on the base of your bottle you cannot tell whether a notice applies to what you are holding.
So three practical things follow. Keep the bottle rather than decanting the capsules into an organiser, because the code goes with the bottle. Note the lot somewhere when it arrives, so you can check without digging the bottle out. And if a notice ever names a lot you hold, stop taking it and call the desk on +1 (302) 200-3480 rather than working out on your own whether it matters.
This desk has had no recall and no adverse-event report on this stock. That is a statement about our own limited order book, not a safety finding, and it should not be read as one.
Every page, every journal post, the bottle facts and the ingredients go through review by Dr. Jennifer Roelands, MD before they ship. We write these pages from the printed Femipro bottle and from the Supplement Facts panel photographed in our own stock images, cite public research for cranberry, bearberry, berberine, mimosa pudica and the named lactobacillus strains, and print “not published” wherever a figure is not disclosed rather than estimating it. This label publishes two blend totals and no individual amount, and that fact appears on every page where an ingredient is named. Where the seller’s marketing claims more than the bottle supports, we say so on the page. Corrections are made on the page itself and the review date moves forward. Write to [email protected]. Last reviewed September 2026 by Dr. Jennifer Roelands, MD.
Sources for Femipro batch verification
- FDA, current good manufacturing practice, 21 CFR part 111. U.S. Food and Drug Administration. Current Good Manufacturing Practices (CGMPs) for Food and Dietary Supplements, listing dietary supplements under 21 CFR part 111. View source
- FDA, questions and answers on dietary supplements. U.S. Food and Drug Administration. Questions and Answers on Dietary Supplements. "Under DSHEA, FDA does not have the authority to approve dietary supplements before they are marketed." View source
- NCCIH, probiotics usefulness and safety. National Center for Complementary and Integrative Health. Probiotics: Usefulness and Safety. National Institutes of Health. View source
- NCCIH, using dietary supplements wisely. National Center for Complementary and Integrative Health. Using Dietary Supplements Wisely. National Institutes of Health. View source
Order Femipro from the desk that can match your lot
Lot FEM-26/FE-4936 on this stock, an order ID on every purchase, and a telephone number that can put the two together.
$49 to $69 a bottle · 60 days to change your mind
Order Femipro On The Official WebsiteOne-time payment, no subscription · free US shipping · 60-day money-back guarantee · lot FEM-26/FE-4936 · tracking and refunds +1 (302) 200-3480