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Under-Eye Filler / Tear Trough Correction

A specialised hyaluronic acid filler injection technique targeting the infraorbital hollow (tear trough) — the depression running from the inner corner of the eye toward the cheek — to reduce under-eye bags, dark circles, and sunken appearance without surgery.

How it works

The tear trough is a ligamentous attachment (orbicularis retaining ligament) where the facial fat compartments separate. Volume loss here creates the classic sunken, hollow, or dark-circle appearance. Ultra-soft HA filler (low G-prime products like Juvederm Volbella or Restylane Eyelight) is placed deep (supraperiosteal) or in the sub-orbicularis plane to restore volume precisely. Cannula technique preferred over needle for safety in this vascular area.

Reported benefits

  • Under-eye hollow and tear trough reduction
  • Dark circle improvement (structural/volume-related cause)
  • Refresh tired appearance without surgery
  • Immediate results with no downtime in most cases
  • Natural-looking rejuvenation
  • Reversible with hyaluronidase enzyme if needed

Regulatory status

European Union· EMA· 2010
Authorized

Approved for: Periorbital volume restoration, Tear trough correction

Tear trough filler is a recognised aesthetic procedure in EU. Multiple CE-marked HA fillers used for this indication. European aesthetic medical societies have published guidelines on safe cannula technique for this high-risk area.

United Kingdom· MHRA· 2010
Approved

Approved for: Periorbital volume restoration and rejuvenation

Recognised aesthetic procedure using MHRA-registered HA filler devices. Health and Care Act 2022 requires this procedure to be performed by licensed medical practitioners. Considered higher-risk due to proximity to ocular vasculature.

United States· FDA· 2023
Off-label use

Approved for: Hyaluronic acid fillers FDA-approved for facial wrinkles (on-label), Periorbital use is off-label for most products (Restylane Eyelight approved 2023)

Restylane Eyelight (Galderma) received FDA approval specifically for infraorbital hollowing in November 2023 — the first HA filler with on-label FDA approval for this indication. Other HA fillers used for tear troughs remain off-label. FDA has warned that periorbital filler carries risk of blindness from inadvertent intravascular injection.

Practical details

Frequency: Every 12–18 months

Results last: Immediate results; swelling peaks at 24–48h; final result at 2 weeks; lasts 12–18 months

Contraindications:

  • Prominent under-eye bags (fat herniation) — filler may worsen this; blepharoplasty may be more appropriate
  • Very thin skin (HA filler Tyndall effect risk — bluish discolouration)
  • Unrealistic expectations about dark circles of pigmentary or vascular origin
  • Recent eye surgery
  • Blood thinning medications
  • Allergy to hyaluronic acid

Always consult a licensed medical professional before undergoing any treatment. This information is educational only and does not constitute medical advice.

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