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Juvederm for Gummy Smile

Written & medically reviewed by the Dermapedia team
At a Glance

Botulinum toxin, not filler, is the better-evidenced treatment for a gummy smile. A gummy smile is usually caused by an upper lip that lifts too far when you smile. Toxin relaxes the small muscles that do the lifting. Filler does not relax a muscle — it adds volume — so for the classic muscular gummy smile it is treating a different thing.

No Juvederm product carries an FDA approval that names a gummy smile or gum show. Juvederm Ultra XC is approved for the lips and perioral area, and Juvederm Volbella XC is approved for the lips and perioral lines. Using either one to change how much gum shows is off-label. Off-label injecting is legal and routine in medicine, but it means no trial was submitted to the FDA for this use.

Lip filler changes a different part of the picture. Adding volume to the upper lip makes the lip itself fuller and can slightly change how much of the gum is visible, but it does not weaken the muscle that raises the lip. Some injectors also place filler higher up, around the base of the nose, to add resistance against that muscle pull. That second technique has only case-series and technique-paper evidence behind it.

Surgery is the third option, and the pooled relapse figures favour it - but they come from separate studies, not from anyone randomising patients between the two. Lip repositioning surgery shortens how far the lip can ride up by altering the tissue inside the upper lip. A 2026 systematic review pooled 17 studies and 576 patients and reported relapse in 70 to 90 percent of cases after toxin alone, 40 to 60 percent after conventional lip repositioning surgery, 20 to 35 percent after modified surgical versions, and 10 to 20 percent after toxin combined with surgery. The included studies are mostly not randomised, so read those as ranges from the literature rather than as a head-to-head result.

The cause decides the treatment, and there is more than one cause. Excessive gum show can come from a hypermobile lip (muscular), from the upper jaw being vertically long (skeletal), from gum tissue that never fully receded off the teeth, or from a short upper lip. Toxin helps the first. It does nothing for the others. That is the single most useful thing to establish before any injection.

Key Facts

Best-evidenced minimally invasive treatmentBotulinum toxin injected into the muscles that lift the upper lip
Juvederm approvals that name gummy smile or gum showNone
Closest Juvederm approvalsJuvederm Ultra XC, lips and perioral area (2015); Juvederm Volbella XC, lips and perioral lines (2016)
Conventional definition of a gummy smileMore than 3 mm of gum visible above the upper front teeth on smiling
Toxin timing in trialsMaximum improvement at 2 to 4 weeks; effect lasting roughly 12 to 24 weeks
Toxin relapse rate, 2026 systematic review70 to 90 percent
Conventional lip repositioning surgery relapse rate40 to 60 percent
Modified lip repositioning surgery relapse rate20 to 35 percent
Toxin plus surgery relapse rate10 to 20 percent
Largest hyaluronic acid filler study for gum show50 patients, mean reduction 2.5 mm, 40 percent of the original gum show returned by 6 months and the effect was gone by 12 months
Only published toxin-versus-filler head-to-head14 patients total, 90 days of follow-up
ReversibilityJuvederm is a hyaluronic acid filler and can be broken down with hyaluronidase

The honest answer, up front

If you have a gummy smile caused by a lip that lifts too far, botulinum toxin is the treatment with the most evidence behind it, and Juvederm is not.

A systematic review of 13 prospective controlled clinical trials found that toxin injected into the lip-elevator muscles reduced gum show from a baseline range of 3.5 to 6.8 mm down to 3 mm or less in most cases, with maximum improvement at 2 to 4 weeks and an effect lasting roughly 12 to 24 weeks. The muscles targeted are the levator labii superioris alaeque nasi, the levator labii superioris and the zygomaticus minor — the small muscles that pull the upper lip up and out when you smile.

That is not the same as saying the evidence is strong: An evidence-based review in 2022 concluded there was "limited evidence, not higher than level III" supporting toxin for gummy smile linked to overactive muscles around the mouth. And no botulinum toxin brand holds an FDA cosmetic indication for a gummy smile either. Botox Cosmetic's cosmetic indications are glabellar lines, lateral canthal lines, forehead lines and platysma bands. Toxin for a gummy smile is off-label too — it is simply better studied.

The filler evidence sits a step below that again. It is mostly cohort studies, case series and technique descriptions, which the papers themselves label Level of Evidence IV.

What a gummy smile actually is — and why the cause changes the answer

Excessive gum display is conventionally defined as more than 3 mm of gum visible above the upper front teeth when you smile. But that single measurement has several different causes, and they do not respond to the same treatment.

Lip hypermobility: The muscles lift the upper lip further than average. This is the muscular type, and it is the type toxin is aimed at.

Vertical maxillary excess: The upper jaw is long, so the teeth and gums sit lower relative to the lip. This is skeletal. Injecting anything into soft tissue does not change bone; the definitive treatment is orthognathic (jaw) surgery.

Altered passive eruption: The gum never fully receded off the teeth as they came in, so the teeth look short and the gum looks large. The dental treatment is crown lengthening.

A short upper lip: An anatomical proportion, not a muscle problem.

Combinations are common. A page, or a clinic, that treats "gummy smile" as one condition with one treatment is going to get it wrong for a large share of people. Working out which of these is driving your smile is the first appointment, not the injection.

Where Juvederm does and does not fit

Two quite different filler ideas get bundled together in clinic copy, and they are worth separating.

1. Lip filler in the upper lip: This is what most people mean. Adding hyaluronic acid to the upper lip increases the amount of red lip (vermilion) on show and can make the lip look fuller and slightly longer. It changes the proportion between lip and gum. What it does not do is reduce how far the muscle lifts the lip when you smile. In someone whose gum show is driven by muscle pull, the muscle keeps pulling.

The relevant approvals here are for lip augmentation, not for gum show: Juvederm Ultra XC has been approved for injection into the lips and perioral area for lip augmentation in adults over 21 since 30 September 2015, and Juvederm Volbella XC has been approved for the lips and perioral lines since 31 May 2016. Note that Juvederm Ultra Plus XC does not hold a US lip indication — its approved wording covers moderate to severe facial wrinkles and folds, such as nasolabial folds.

2. Filler higher up, as "myomodulation": Here hyaluronic acid is placed in the premaxillary or paranasal area — around and above the base of the nose — either to add physical resistance against the lifting muscles, or to support a flat, deficient area under the nose. The published work behind this is expert clinical experience and case series, labelled Level of Evidence IV by the authors themselves, not trial evidence.

Neither use is FDA-approved for a gummy smile: No US hyaluronic acid filler carries an indication that names gum show or upper lip elevation.

What the filler evidence actually shows

The best single filler study is a cohort of 50 patients using a hyaluronic acid infiltration technique, 0.1 mL per injection point. Mean reduction in gum show on smiling was 2.5 mm, stable from one week. Satisfaction was 82.1 percent, and every patient said they would recommend it. The authors declared no conflicts of interest.

The durability finding in the same study is the one to hold on to: 40 percent of the original gum show had come back by 6 months, and the effect was completely gone at 12 months: That was a cohort with no control arm, so improvement over time cannot be separated from the natural course, but it is the clearest published picture of how long this lasts.

There is exactly one published head-to-head of botulinum toxin against hyaluronic acid filler for gummy smile. It enrolled 14 patients in total — about seven per arm — with 90 days of follow-up, at a single centre, with no stated blinding or randomisation method and no brands or doses reported. It reported that toxin gave immediate improvement while filler gave more consistent and prolonged results with higher satisfaction. A 14-patient study is not enough to establish that filler beats toxin here, and it should not be read that way. It is worth knowing the study exists, and worth knowing how small it is.

A note on toxin doses, and why no number here carries a brand

Botulinum toxin units are not interchangeable between brands. Every FDA toxin label says so explicitly: units of Dysport cannot be converted into units of any other product, and the same wording appears on the Jeuveau, Daxxify and Letybo labels. A dose figure without a brand name attached is not a usable dose.

That is a real problem in this literature. The gummy smile trials do not consistently name which toxin brand they used. A double-blind randomised trial of 49 patients compared injecting at the "Yonsei point" against conventional injection into the levator labii superioris alaeque nasi, using a total of 6 units split 3 units per side — but the brand is not stated, so those units belong to no scale. Another randomised preliminary trial compared four injection points against two, at 2 units per point, and again did not name the brand. The 2026 systematic review reports doses of 2 to 7.5 units per side across its included studies with the brand unspecified.

So the pattern is consistent — small doses, into one or two lip-elevator muscles — but there is no brand-anchored dose you can quote: If you are told a number at a consultation, the question worth asking is which brand's units it is in.

Two findings from those trials are useful anyway. The 49-patient randomised trial found gum show reduced at 4, 12 and 24 weeks and back to baseline at 48 weeks in both groups, with no difference between them — so the more fashionable injection point was not better. It was funded by the National Natural Science Foundation of China and a university hospital, not by a manufacturer. The other trial found that adding injection points prolonged the effect (about 25 weeks versus 16 weeks) but did not make it stronger; its authors call their own results preliminary because of high dropout.

Surgical lip repositioning, and how the three options compare

Lip repositioning surgery removes a strip of tissue from inside the upper lip and reattaches the lip lower down, limiting how far it can ride up. It is done under local anaesthetic, usually by an oral surgeon or periodontist.

The best comparative source is a 2026 systematic review of 17 studies and 576 patients — 179 treated with toxin alone, 317 with lip repositioning surgery and 80 with both.

Botulinum toxin alone: Baseline gum show 5.1 to 6.9 mm, peak reduction 3.0 to 4.2 mm, relapse 70 to 90 percent

Conventional lip repositioning surgery: Baseline 4.8 to 6.2 mm, peak reduction 3.5 to 4.5 mm, relapse 40 to 60 percent

Modified surgery: (adding a small muscle cut or anchoring stitches to the bone lining): relapse 20 to 35 percent

Toxin combined with surgery: relapse 10 to 20 percent

The review reported no major adverse effects across all three. Its limits matter: the included studies are heterogeneous, mostly not randomised, and the toxin brand is again unspecified. Surgery is also not reversible in the way an injection is, it leaves a scar inside the lip, and it does nothing for a skeletal cause.

The risks that belong to filler in this area

Every filler risk applies, plus two things specific to the region.

The area around the base of the nose is a vascular danger zone: The angular and facial arteries run there, and they connect back to the arteries that supply the eye. If filler is pushed into one of those arteries it can travel backwards and then forwards into the retinal circulation. In a review of 511 published cases of blindness after filler spanning more than a century, the nose accounted for 40.6 percent of the 365 most recent cases, the forehead 27.7 percent and the glabella 19.0 percent. Of 318 cases with a documented outcome, 6.0 percent recovered completely, 25.8 percent improved partially and 68.2 percent did not recover. These are counts of published cases, not a rate — nobody knows how many injections are performed, so this cannot be turned into a personal percentage. What it does establish is that when it happens, it is usually permanent.

Filler does not address muscle overactivity at all: In the classic hypermobile-lip patient it is treating the wrong mechanism, which is a reason results can disappoint even when the injection itself goes perfectly.

The ordinary risks are bruising, swelling, tenderness, lumps and asymmetry. In FDA pivotal trials of hyaluronic acid fillers these injection-site responses were common and mostly settled within a week.

One thing does work in filler's favour: Juvederm is hyaluronic acid, so it can be broken down: An injection of hyaluronidase, an enzyme that splits hyaluronic acid, dissolves it — usually within minutes to hours. That is also the emergency treatment if a blood vessel is blocked. Two caveats belong beside it. Dissolving filler is an off-label use of hyaluronidase in the US: the Hylenex label lists only fluid administration, drug dispersion and urography as approved uses. And hyaluronidase is not a reliable rescue for filler-related blindness — in the 511-case review, no treatment showed a statistically significant association with visual improvement.

Questions worth asking at a consultation:

Which cause of gum show do you think I have — muscle, jaw, gum tissue, or lip length?

If it is muscular, why would you inject filler rather than toxin?

If you are recommending toxin, which brand and how many of that brand's units?

What is the plan if the result is asymmetric or my lip feels heavy?

Do you stock hyaluronidase on site?

Would a dental or oral surgery opinion change what we do?

Get emergency help now

Go to an emergency department or call 911 if any of these happen during or after an injection. They can mean filler has entered a blood vessel, and time is measured in hours.

Any change in vision: Blurring, a dark patch, double vision or loss of sight in one eye

Sudden severe pain, or pain out of proportion to the injection

Skin turning white (blanching), then dusky, purple, grey or net-like and mottled

Weakness, drooping, slurred speech, confusion or any other stroke-like symptom

Do not wait for a routine appointment and do not wait to see if it settles overnight.

Call your injector if

Swelling keeps growing after the first few days instead of settling

A lump appears and does not soften over a couple of weeks

Redness spreads outward from the injection site

Tenderness, firmness or swelling appears weeks or months later, which can be a delayed inflammatory reaction or an infection

Your smile is noticeably uneven, or the upper lip feels heavy or hard to control

The filler seems to have moved from where it was placed

Questions people ask

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Does Juvederm fix a gummy smile?Not directly, and it is not approved for it. No Juvederm product carries an FDA indication naming gum show. Lip filler makes the upper lip fuller and changes the proportion between lip and gum, but it does not reduce how far the muscle lifts the lip. For a gummy smile caused by a hypermobile lip, botulinum toxin is the better-evidenced option.
Why do clinics offer filler for it then?Because filler genuinely changes the look of the upper lip, because some patients want fuller lips anyway, and because there is a described technique of placing hyaluronic acid higher up to add resistance against the lifting muscles. That technique exists in the literature, but as case series and expert experience rated Level of Evidence IV — not as trials.
Is botulinum toxin approved for a gummy smile?No. Botox Cosmetic's cosmetic indications are glabellar lines, lateral canthal lines, forehead lines and platysma bands; the other US toxin brands are narrower still. Toxin for a gummy smile is off-label. Off-label use is legal and routine — the point is that toxin has 13 prospective controlled trials behind this use and filler does not.
How long does each option last?In the toxin trials, maximum improvement came at 2 to 4 weeks and the effect lasted roughly 12 to 24 weeks, with gum show back at baseline by 48 weeks in one randomised trial. In the largest filler cohort, 40 percent of the original gum show had returned by 6 months and the effect was completely gone at 12 months. Surgery lasts longest but still relapses in 40 to 60 percent of conventional cases.
Can I have toxin and filler together?That combination is described in the literature, and toxin combined with lip repositioning surgery had the lowest relapse rate in the 2026 systematic review, at 10 to 20 percent. No adequately sized trial has tested toxin plus filler specifically for gum show. The only direct toxin-versus-filler comparison enrolled 14 patients in total.
What if my gummy smile is from my jaw and not my lip?Then neither toxin nor filler will change it. Vertical maxillary excess is a skeletal difference, and the definitive treatment is orthognathic surgery. Gum tissue that never receded off the teeth is treated by crown lengthening. This is why identifying the cause first matters more than choosing a product.
Can Juvederm be removed if I do not like the result?Yes. Juvederm is a hyaluronic acid filler, and hyaluronidase breaks hyaluronic acid down, usually within minutes to hours. In the US this is an off-label use of the enzyme — the Hylenex label does not list filler dissolution among its approved uses. Repeat dosing is common, and firmer, more heavily cross-linked products need more of it.
What is the most dangerous thing that can go wrong?Filler entering an artery. Around the base of the nose, those vessels connect back to the eye's blood supply. A review of 511 published cases of blindness after filler found that of 318 cases with a recorded outcome, 68.2 percent had no recovery of vision. It is rare, but it is a same-hour emergency, and sudden vision change after an injection means an emergency department, not a phone call.

References

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Cabral M, et al. Gummy Smile: Comparison Between Botulinum Toxin, Lip Repositioning Surgery and Combined Techniques in Cases of Lip Hypermobility — A Systematic Review. Oral. 2026;6(2):49. https://www.mdpi.com/2673-6373/6/2/49
Systematic review of 17 studies and 576 patients (toxin alone 179, lip repositioning surgery 317, combined 80). Source of the relapse figures and the peak-reduction ranges. Included studies are heterogeneous and mostly not randomised, and the toxin brand is not specified, so its unit figures cannot be attributed to any product.
Systematic review of botulinum toxin for excessive gingival display. Toxicon. 2024. https://pubmed.ncbi.nlm.nih.gov/39134226/
Thirteen prospective controlled clinical trials. Source of the 2 to 4 week peak, the roughly 12 to 24 week duration, the target muscles, and the reduction from a 3.5 to 6.8 mm baseline to 3 mm or less. The review does not state which toxin brands the included studies used.
Application of botulinum toxin at the Yonsei point for the treatment of gummy smile. Plast Reconstr Surg. 2024. https://pubmed.ncbi.nlm.nih.gov/37166037/
Double-blind single-site randomised trial, 49 patients, follow-up to 48 weeks. Gum show fell at 4, 12 and 24 weeks and returned to baseline at 48 weeks in both arms, with no difference between injection techniques. Funded by the National Natural Science Foundation of China and a university hospital — not industry. The toxin brand is not stated in the abstract.
Costa AB, et al. Randomised controlled preliminary trial of injection points for excessive gingival display. Aesthet Surg J. 2022. https://pubmed.ncbi.nlm.nih.gov/34533189/
Four injection points versus two, 2 units per point. More points prolonged the effect (about 25 weeks versus 16 weeks) without increasing its magnitude. The authors label the results preliminary because of high dropout, and the brand is not stated.
Evaluation of a New Technique of Gingival Smile Reduction after Hyaluronic Acid Infiltration: A Cohort Study. Dent J (Basel). 2024. https://pubmed.ncbi.nlm.nih.gov/39452457/
Cohort of 50 patients, 0.1 mL per injection point, mean reduction 2.5 mm, satisfaction 82.1 percent. Forty percent of the original gum show returned by 6 months and recovery was complete at 12 months. No control arm. Authors declare no conflicts of interest. Also the source of the more-than-3 mm definition used here.
Comparative study of botulinum toxin type A versus hyaluronic acid filler for gummy smile. J Pharm Bioallied Sci. 2025. https://pubmed.ncbi.nlm.nih.gov/41164612/
The only published head-to-head. Fourteen patients in total, 90 days of follow-up, single centre, no stated blinding or randomisation method, brands and doses not reported. Far too small to establish which treatment is better.
Botulinum toxin type A for gummy smile: an evidence-based review. Evid Based Dent. 2022. https://pubmed.ncbi.nlm.nih.gov/35710887/
Concluded there is "limited evidence, not higher than level III" supporting botulinum toxin effectiveness for gummy smile associated with overactive perioral muscles.
Hyaluronic Acid Myomodulation in the Treatment of Gummy Smile. Aesthetic Plast Surg. 2025. https://pubmed.ncbi.nlm.nih.gov/39815021/
Describes placing hyaluronic acid to add resistance against the lip-elevator muscles. Rated Level of Evidence IV by the authors — technique and clinical experience, not a controlled trial.
US Food and Drug Administration. PMA P050047/S044, Juvederm Ultra XC, approved 30 September 2015. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P050047S044
The lip approval. Indicated for injection into the lips and perioral area for lip augmentation in adults over the age of 21, and into the mid to deep dermis for moderate to severe facial wrinkles and folds. Nothing about gum show. The supplement applies to Ultra XC, not to Ultra Plus XC.
US Food and Drug Administration. PMA P110033/S018, Juvederm Volbella XC, approved 31 May 2016. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P110033S018
Indicated for injection into the lips for lip augmentation and for correction of perioral lines in adults over the age of 21.
US Food and Drug Administration. BOTOX Cosmetic (onabotulinumtoxinA) prescribing information, revised October 2024. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/103000s5316s5319s5323s5326s5331lbl.pdf
The cosmetic indications are glabellar lines, lateral canthal lines, forehead lines and platysma bands. No gummy smile indication.
US Food and Drug Administration. DYSPORT (abobotulinumtoxinA) prescribing information, revised September 2023. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/125274s125lbl.pdf
Contains the standard labelling statement that potency units of one botulinum toxin product cannot be compared to or converted into units of any other.
Doyon VC, et al. Update on Blindness From Filler: Review of Prognostic Factors, Management Approaches, and a Century of Published Cases. Aesthet Surg J. 2024;44(10):1091-1104. https://pubmed.ncbi.nlm.nih.gov/38630871/
511 published cases since 1906. Among the 365 most recent, the nose accounted for 40.6 percent, forehead 27.7 percent and glabella 19.0 percent; hyaluronic acid was the material in 79.6 percent. Of 318 cases with recorded outcomes, 6.0 percent recovered completely and 68.2 percent did not recover. No treatment was significantly associated with improvement. A literature case count with no denominator, so it cannot give a rate.
Jones DH, et al. Preventing and Treating Adverse Events of Injectable Fillers: Evidence-Based Recommendations From the American Society for Dermatologic Surgery Multidisciplinary Task Force. Dermatol Surg. 2021;47(2):214-226. https://www.asds.net/Portals/0/PDF/asdsa/Preventing%20and%20Treating%20Adverse%20Events%20of%20Injectable%20Fillers%20Evidence-Based%20Recs%20From%20ASDS%20Task%20Force%20Article.pdf
Consensus task force guidance. Stop injecting on blanching or blood in the syringe; treat skin occlusion with high-dose hyaluronidase; contact emergency stroke services for any central nervous system signs. The task force grades its own blindness-treatment recommendation as conditional, low certainty evidence.
US Food and Drug Administration. Dermal Fillers (Soft Tissue Fillers). https://www.fda.gov/medical-devices/aesthetic-cosmetic-devices/dermal-fillers-soft-tissue-fillers
FDA's risk list — common bruising, redness, swelling, pain and tenderness; rarer nodules, infection and blood vessel injury causing necrosis, blindness or stroke — and its note that side effects can appear weeks, months or years after injection.
US Food and Drug Administration. HYLENEX recombinant (hyaluronidase human injection), prescribing information. https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&varApplNo=021859
The approved indications are limited to subcutaneous fluid administration for hydration, increasing the dispersion and absorption of other injected drugs, and subcutaneous urography. Dissolving dermal filler is not among them, which is why that use is off-label.
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