Official product information
Medical Disclaimer and Earnings Disclosure
Nothing here is medical advice. The statutory framing, the four groups the warning panel names, and why a new symptom is a reason to see a clinician.
Written and reviewed by the Maxforce Editorial Desk · Last updated October 29, 2026
Quick answer
FDA does not assess a dietary supplement before it is marketed, which is why the jar prints the required disclaimer in its own ruled box, tied by asterisk to all three front claims. Nothing on this site diagnoses, treats, cures or prevents anything. A new or worsening sexual symptom can be the first sign of a cardiovascular or endocrine problem, and is a reason to see a clinician.
3 front claims, one ruled box
The statutory framing, and the box the label prints it in
Nothing in this aisle is assessed before it is sold, which is why the sentence in the ruled box is required.
Start with the statutory framing, because it explains the sentence printed on the jar.
Supplements are not assessed before they go on sale
FDA states it in one line: “Under DSHEA, FDA does not have the authority to approve dietary supplements before they are marketed.” So a company may put a supplement on the market without anyone reviewing it first, it is responsible for holding evidence that its product is safe and its label truthful, and FDA’s powers are mostly exercised after sale.
Which is why the printed disclaimer exists
Printed on the label, in its own ruled box
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
Give the label credit for how it prints it
The front of this jar makes three claims and hedges every one: May Support: Vitality*, Drive*, Performance*. Each carries an asterisk, the asterisk resolves to the box above, and the box sits on the same wrap, ruled off from everything around it. That is the correct construction.
0 diagnoses made on this website
This site is information, not advice
This is a product information website. It is not a clinic and not a pharmacy, and nobody writing it is your doctor, pharmacist or dietitian.
Nothing here is medical advice
Nothing on these pages is a diagnosis, a treatment recommendation, a dosing instruction for your situation or advice about a medicine you take. Nothing here diagnoses, treats, cures or prevents anything. These pages transcribe a label, quote federal consumer pages and date them, and do arithmetic anybody can repeat. They cannot know your history, and they are no substitute for somebody who can.
And the federal record says what it says
NCCIH: “No complementary health approaches have been shown to be safe and effective for sexual enhancement or treating erectile dysfunction (ED).” Two of the nine ingredients on this panel have a federal consumer page; five have none.
If something feels wrong, stop
Do not wait to see whether it settles. Stop taking the gummy and speak to a clinician. The label’s own instruction says the same, and it is quoted below.
2 systems a symptom can point at
A new or worsening symptom is a reason to see somebody
This is the most important section on this page, and it has nothing to do with the product.
A new or worsening symptom is a reason to be examined
MedlinePlus: “ED can be a sign of health problems. It may mean your blood vessels are clogged. It may mean you have nerve damage from diabetes.” And: “If you don’t see your doctor, these problems will go untreated.” Clogged blood vessels are cardiovascular and diabetes is endocrine, so sexual difficulty can be the first visible sign of something worth treating in its own right. That is a reason to have it looked at rather than a reason to be embarrassed.
There is nothing awkward about the appointment
MedlinePlus is direct: “Some people have trouble speaking with their doctors about sex. But if you have ED, you should tell your doctor.” A clinician hearing this is hearing about a common problem with known causes and known treatments. On when to go: “If problems last more than a few months or cause distress for you or your partner, you should see your health care provider.”
And why a supplement is the wrong first move
A delay is the real harm in this category far more often than an ingredient is. If you are choosing between a gummy and an appointment, make the appointment.
4 groups the warning panel names
The label’s own warning panel, and the interaction question
The label prints its own warning panel, it names the right four groups, and it is reproduced here word for word.
The warning panel, verbatim
WARNING: If you are pregnant or nursing, take medications or have a medical condition, consult your doctor before using. Discontinue use and consult your doctor is any adverse reactions occur.
It also carries a typo in its last sentence, where the word should be if rather than is. The panel is still a real one.
The four groups
Pregnancy and nursing. This product is for Adults 18 and over. NCCIH on one of its ingredients: “Ashwagandha should be avoided during pregnancy and should not be used while breastfeeding.” Medication. Take the jar to a pharmacist rather than guessing. A medical condition. NCCIH, on a product aimed at older men: “Because ashwagandha may increase testosterone levels, people with hormone-sensitive prostate cancer should avoid its use.”
The interaction with a medicine attached to it
NCCIH names one: “Green tea at high doses has been shown to reduce blood levels and, therefore, the effectiveness of the drug nadolol, a beta-blocker used for high blood pressure and heart problems.” Green tea extract is row four of nine here. Because FDA requires blend members to be listed in descending order of predominance by weight, and because caffeine is printed at 5 mg in row five, row four is at least 5 mg and no more than 62 mg, while ashwagandha at row six is 5 mg or less. Both are far below the amounts in the reports, and neither fact substitutes for telling somebody with your chart in front of them that you are taking this.
5 mg of caffeine against 400 a day
Caffeine, added sugar, and what to do if something goes wrong
Two specifics that belong on a disclaimer for this jar, and then what to do if something goes wrong.
The caffeine and the added sugar
Caffeine is declared and itemised at 5 mg, to the label’s credit, and a rounding error beside FDA’s reference figure: “For most adults, the FDA has cited 400 milligrams a day — that’s about two to three 12-fluid-ounce cups of coffee — as an amount not generally associated with negative effects.” The caveat still applies to anyone who reacts strongly: “However, there is wide variation in both how sensitive people are to the effects of caffeine and how fast they eliminate it from the body.” The green tea extract above it carries caffeine of its own, with no second figure printed. Each gummy also carries 3 g of sugar, all of it added — 6% of the Daily Value, in 10 calories, one a day, every day.
What is not published, and what that means
Eight of the nine amounts are not printed, so no page here can tell you whether this gummy contains enough of anything to matter. Do not read a named ingredient as a quantity of it.
If you have a reaction, here is the order to do things in
Stop taking it, which is the label’s own instruction. Tell a clinician or a pharmacist and take the jar, because the panel is legible. Then tell the company: no adverse-event reporting address is printed on this label or supplied with the pack, so the routes that exist are the number beside the distributor’s name, 888-338-0317, and the sales line, +1 (302) 200-3480.
Questions
Maxforce FAQ: disclaimer questions
Is Maxforce FDA-approved?
No, and no supplement is. FDA: “Under DSHEA, FDA does not have the authority to approve dietary supplements before they are marketed.” The “Registered FDA Facility” seal refers to a factory filing, not to this product.
Is this product on any FDA list of tainted products?
A search of FDA’s Sexual Enhancement and Energy Product Notifications on September 25, 2026 did not return Maxforce. That is a statement about what a database contained on a date and nothing more. FDA itself notes: “FDA is unable to test and identify all products marketed as dietary supplements that have potentially harmful hidden ingredients.” No test result for this product exists in the public record.
Should I tell my doctor?
Yes. NIH ODS: “Tell your health care providers (including doctors, dentists, pharmacists, and dietitians) about any dietary supplements you’re taking.” Take the jar — the panel is legible and it is the useful thing to hand over.
References
Sources for this page
- U.S. Food and Drug Administration. Questions and Answers on Dietary Supplements. www.fda.gov. Accessed September 25, 2026.
- National Center for Complementary and Integrative Health. Dietary Supplements Marketed for Weight Loss, Bodybuilding, and Sexual Enhancement: What the Science Says. www.nccih.nih.gov. Accessed September 25, 2026.
- National Center for Complementary and Integrative Health. Ashwagandha: Usefulness and Safety. www.nccih.nih.gov. Accessed September 25, 2026.
- National Center for Complementary and Integrative Health. Green Tea: Usefulness and Safety. www.nccih.nih.gov. Accessed September 25, 2026.
- MedlinePlus, U.S. National Library of Medicine. Erectile Dysfunction. medlineplus.gov. Accessed September 25, 2026.
- U.S. Food and Drug Administration. Spilling the Beans: How Much Caffeine is Too Much?. www.fda.gov. Accessed September 25, 2026.
Next
Keep reading
Safety, cautions and interactions
Every published caution covering anything in this jar, and the five blanks.
Read it →Who it is for, and who should stop
Three situations where it makes sense and six where it does not.
Read it →Terms and conditions
What this site is, and whose contract your order actually is.
Read it →Read what is published about Maxforce before you order
30 gummies a jar, one a day, thirty days a jar. Nine ingredients inside 82 mg, with only the caffeine itemised at 5 mg. Sales line +1 (302) 200-3480. Talk to a health care professional before starting anything new.
Price shown at checkout · 60-day window from the date of purchase · ships from inside the US · sales line +1 (302) 200-3480