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Treatment areas atlas

Botox areas of the face: why, how and for whom, area by area

In France, botulinum toxin is approved for aesthetic use in only three areas of the face: frown lines and, depending on the product, crow’s feet and forehead lines. Other areas are off-label uses. This atlas covers eleven areas: what the toxin treats, with which toxin, and what to ask your doctor.

This atlas answers three questions, area by area: why is this area treated, with which toxin, and for whom? It is based on the official product labels and on medical publications, with no promise of results. It complements our general page to understand botulinum toxin and does not replace a consultation.

Key points

  • In France, botulinum toxin is approved for aesthetic use only for frown lines and, depending on the product, crow’s feet and forehead lines2,3,4,5.
  • The short-acting botulinum toxin (serotype E) is approved for frown lines only: in the European Union and Canada1,11.
  • The eight other areas of the atlas are not in any French label: any injection there is off-label and should be discussed as such with your doctor.
  • The effect is always temporary: usually 3–4 months with a type A toxin, 2–3 weeks with the short-acting botulinum toxin (serotype E)1,2.

The eleven areas of the atlas

Interactive atlas

Choose an area of the face

Tap an area to find out why it is treated, with which toxin, and what the official product labels say.

Tap an area of the face

Front-view illustration of a face, from the forehead to the neck, with the atlas areas outlined

Choose an area

Forehead

Long-acting botulinum toxin (type A)
Approved for aesthetic use in this area (SmPC in force in France)
Short-acting botulinum toxin (serotype E)
No aesthetic indication for this area in the SmPCs in force in France: off-label use, to be discussed with your doctor

Depending on the product: not every type A toxin approved for aesthetic use covers this area.

Each area has its own "why and how" page, built on the same outline: the muscle involved, what the toxin does and does not treat, the approval status, who it is for, onset and duration, and risks.

The upper face:

  • Forehead lines: the frontalis muscle, approved for some type A toxins.
  • Frown lines: the creases between the eyebrows, the only area approved for both families of toxins.
  • Eyebrows: lifting the tail of the eyebrow, off-label.
  • Eyelids: an area that is protected, and why.
  • Crow’s feet: the lines at the corner of the eye, approved for some type A toxins.

The mid and lower face, and the neck:

How does botulinum toxin work on an area?

Botulinum toxin is injected into a muscle. It blocks the release of a chemical messenger, acetylcholine, at the junction between nerve and muscle, by cleaving a protein called SNAP-251. The injected muscle receives fewer signals and contracts less, locally and temporarily. The effect wears off as the nerve endings recover their function1.

This explains what the toxin can do, and what it cannot. It softens lines that deepen when a muscle contracts: frowning, raising the eyebrows, squinting when you smile. It can also change the balance between opposing muscles, as in the eyebrow lift. On the other hand, it does not add volume, does not tighten the skin and does not act on lines caused only by skin quality. Each page states these limits for its area.

Approved or off-label: what difference does it make?

A medicine is approved for specific indications, written in its official label, called the summary of product characteristics (SmPC). For aesthetic use, all type A botulinum toxins marketed in France carry the "frown lines" indication; some also cover crow’s feet, others forehead lines2,3,4,5,6,7. All these indications share the same condition: moderate to severe lines whose severity has an important psychological impact, in adults2,4,5.

The other areas of the atlas are not in any French label: nose, gummy smile, lips, chin, masseter, neck, and eyebrow lift2,4,5. An injection in these areas is an off-label use. In practice, the label then gives no dose, no timeline and no efficacy data for the area: the doctor relies on published studies and expert consensus, whose level of evidence varies from one area to another. Your doctor should tell you so.

The status may differ from one country to another. For example, in October 2024 the FDA approved a type A toxin for neck bands in the United States; this approval does not apply in France10. Each page shows the status of its area in a dated table.

Which toxin for which area?

Two families of botulinum toxins are now approved for aesthetic use in the European Union. Long-acting toxins (type A) have been used for aesthetic purposes in France since 20033. The short-acting toxin (serotype E) has been approved in the European Union since 15 July 20268, for a single indication: frown lines in adults1. As of 29 September 2026, the date of the latest update consulted, it had no entry yet in the French public medicines database3.

Outside the European Union, its status differs. It was approved in Canada on 22 June 2026, for the same indication11.

In practice:

  • Frown lines: both families are approved1,3.
  • Crow’s feet and forehead: some type A toxins only2,4,5,6.
  • All other areas: no toxin is approved in France.

The two families do not have the same profile: one works faster and for a shorter time, the other more slowly and for longer. Neither is better than the other, and no trial compares them directly. The short-acting toxin gives you an additional choice for frown lines, to be made with your doctor. To find out more, see the page on the new botulinum toxin and what sets it apart.

Is it right for me? Questions common to every area

Whatever the area, some rules are shared. The approved indications concern adults1,2. The labels contraindicate injection in case of allergy to the toxin or to a component of the product, a generalised disorder of the muscles and of the junction between nerve and muscle (myasthenia gravis, Lambert-Eaton syndrome), or an infection at the injection site1,2,4,5. Treatment is not recommended during pregnancy or breastfeeding1,2. Injection is not recommended in people with a history of swallowing difficulties1,2.

Age matters too, with no single rule. Several type A toxins are indicated only in adults under 654,5,6, one up to 757, and for others data are limited beyond 652. For the short-acting toxin, only 7% of trial patients were 65 or older, with lower response rates1.

Finally, how much the lines bother you is part of the indication: this is not a routine procedure. Your doctor will assess the area at rest and in motion, your medical history, your treatments and your expectations.

What happens during a session?

The toxin is injected into the muscle, at a few points, by a qualified and experienced doctor1. Doses are expressed in units, but the units of one product are not interchangeable with those of another1,2: this is why this site never gives a dose. The name and batch number of the product injected should be recorded, for traceability1,2.

With a type A toxin, one label provides for a review one month after the first session if no improvement is seen, and for a second session to be considered only in the absence of side effects2. Sessions are at least 3 months apart2,4. For the short-acting toxin, the label provides for occasional use; a new injection less than 6 weeks after the previous one has not been evaluated1.

Onset and duration, in brief

For the approved areas, the labels give precise benchmarks:

  • Long-acting toxins (type A): first effects usually within 2–3 days, up to one week; peak effect between week 2 and week 4; usually lasts 3–4 months, up to 6 months depending on the product2,4,6,7,9.
  • Short-acting toxin (serotype E) (frown lines only): first effects from 8 hours, peak effect around day 7, lasts 2–3 weeks1.

For off-label areas, the labels give no timeline. The pages concerned report what studies show when they exist, and say so when no reliable data could be found.

What are the risks, whatever the area?

The labels describe injection-site reactions: pain, swelling, redness, a small bruise1. Headaches are common with some toxins2. A severe allergic reaction can occur very rarely1,2. Each area then has its own risks: a drooping eyelid or eyebrow in the upper face, a changed smile in the lower face, for example. They are temporary and detailed on each page.

The labels also point out that the effect of the toxin can, rarely, spread beyond the injection site: any difficulty swallowing, speaking or breathing requires immediate medical attention1,2.

If something unexpected happens after an injection, our second atlas, devoted to problems after a botulinum toxin injection, covers the same areas and explains, problem by problem, what is happening, how long it lasts and when to see a doctor.

What the toxin does not treat: when to think of something else

Botulinum toxin acts on a muscle, and only on a muscle. Many requests about the face are therefore not a matter for it, and saying so is part of honest information.

  • A line visible at rest, without any movement, is mostly related to the skin: the toxin softens it less than a line that deepens with movement.
  • A loss of volume (cheeks, temples, lips) cannot be corrected by relaxing a muscle.
  • Excess skin, heavy eyelids, under-eye bags or sagging of the lower face call for other approaches.
  • A gummy smile caused by the shape of the jaw, or a wide jaw caused by the bone, does not depend on a muscle.

In these situations, other treatments exist, medical, surgical or dental depending on the case. This site does not cover them, because it is devoted to botulinum toxin: talk to your doctor, who can refer you. Each page of the atlas states, in its first section, what the toxin does not do in that area.

Questions to ask your doctor

Before an injection, whatever the area, these questions will help you decide with full information:

  1. Is this area approved for the product you are offering me, or is it an off-label use?
  2. Which toxin will you use, and why this one?
  3. What result is reasonable in my case, and after how long?
  4. How long should the effect last?
  5. Which side effects should I watch for, and whom should I contact if they occur?
  6. Do my medical history, my treatments or a pregnancy plan raise any issue?
  7. What alternatives exist for what I want to correct?

The answers to these questions are yours: they depend on your face, your health and your expectations, and only a doctor who examines you can give them.

Frequently asked questions

  • Which areas of the face are approved for botulinum toxin in France?

    For aesthetic use, French product labels cover only three areas: frown lines, for every approved toxin, and depending on the product, crow’s feet and forehead lines2,3,4,5. The short-acting botulinum toxin (serotype E) is approved for frown lines only1. The nose, gummy smile, lips, chin, masseter, neck and eyebrow lift are off-label.

  • Which toxin for which area?

    For frown lines, both families are approved: type A toxins and the short-acting toxin1,3. For crow’s feet and the forehead, only some type A toxins have the indication2,4,5. For the other areas, no toxin is approved in France. Each page of the atlas shows this status, area by area, and your doctor chooses the product during a consultation.

  • What does "off-label" mean?

    It means the medicine is used for an area or an indication that is not in its official label. For these uses, the label gives no dose, no timeline and no efficacy or safety data specific to the area. Your doctor should tell you so and explain which data they rely on.

  • How long does the effect of botulinum toxin last?

    With type A toxins, the effect usually lasts 3–4 months, up to 6 months depending on the product2,6,9. With the short-acting toxin, approved only for frown lines, it usually lasts 2–3 weeks1. For off-label areas, the labels give no duration: each page of the atlas reports what studies show, when they exist.

  • Is botulinum toxin right for me?

    No web page can decide that for you. The labels restrict the approved indications to adults with moderate to severe lines that have an important psychological impact1,2, and they list contraindications. Your age, medical history, current treatments and any pregnancy plans also matter. The decision is made with your doctor, during a consultation.

Sources

  1. 1.Summary of product characteristics of the serotype E botulinum toxin approved in the European Union (EPAR annex I) (opens in a new tab) — European Commission (Union Register of medicinal products)
  2. 2.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 68150775) (opens in a new tab) — French public medicines database (BDPM)
  3. 3.French public medicines database: list of medicinal products (CIS file), updated 29 September 2026 (opens in a new tab) — French public medicines database (Ministry of Health)
  4. 4.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 66865211) (opens in a new tab) — French public medicines database (BDPM)
  5. 5.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 61592762) (opens in a new tab) — French public medicines database (BDPM)
  6. 6.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 65066375) (opens in a new tab) — French public medicines database (BDPM)
  7. 7.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 69878363) (opens in a new tab) — French public medicines database (BDPM)
  8. 8.European public assessment report (EPAR) of the serotype E botulinum toxin (opens in a new tab) — European Commission (Union Register of medicinal products)
  9. 9.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 69497348) (opens in a new tab) — French public medicines database (BDPM)
  10. 10.Manufacturer press release (AbbVie) on the FDA approval for neck (platysma) bands, 18 October 2024 (opens in a new tab) — AbbVie (manufacturer)
  11. 11.Canadian product monograph of the serotype E botulinum toxin (authorization date: 2026-06-22) (opens in a new tab) — Health Canada
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