Profhilo Body
IBSA
This is the Profhilo Body identity captured in the dated Aesthetic Pass operational catalogue snapshot. Product-specific source verification is available at family level only.
Evidence status: Catalogue identity · family sources available
The clinical research edition
Go deeper into the formulation and evidence
Explore composition, mechanism, safety and study interpretations for the exact presentation below. These new clinical drafts have a separate review process; this identity profile’s approval does not extend to them.
Identity record
What is recorded
- Record type
- Operational catalogue identity
- Recorded maker
- IBSA
- Classification
- Skin booster / biostimulator
- Material identity
- Not recorded in this snapshot
- Snapshot date
- 15 August 2026
Manufacturer and category are catalogue fields. They are not, by themselves, a regulatory classification or verification of the exact marketed presentation.
Family evidence available
This identity maps to Profhilo
The family profile provides aliases and official family-level sources. Those sources do not automatically verify this exact variant, formulation, label, or market status.
Open family profileProvenance
Family-level sources
These sources support the linked family profile, not every property of this exact catalogue identity.
- ManufacturerOpen source ↗
1. Profhilo product line
IBSA Derma · International overview
Supports: Profhilo family identity and hyaluronic-acid material class.
- ManufacturerOpen source ↗
2. Profhilo — Face & Neck
IBSA Germany · Germany
Supports: German manufacturer product listing and local product-information context.
- RegulatorOpen source ↗
3. PROFHILO 3.2% — ARTG 387132
Australian Therapeutic Goods Administration · Australia
Supports: The active Australian Class III medical-device record for the named PROFHILO 3.2%, 32 mg H-HA plus 32 mg L-HA per 2 ml presentation and its manufacturer.
- Instructions for useOpen source ↗
4. Profhilo — Australian Instructions for Use
IBSA Farmaceutici Italia / IBSA Derma Australia · Australia
Supports: The product-specific Profhilo identity, 2 ml presentation, sodium-hyaluronate composition, professional-use context, precautions, and adverse-event wording for the attached Australian IFU.
Use boundary
What this record does not establish
- Regulatory statusOnly within a source's named jurisdiction; family evidence does not establish status elsewhere.
- Authenticity or supply chainA catalogue name cannot authenticate an individual box, lot, or seller.
- Clinical suitabilityNo product selection, patient assessment, dose, protocol, or injection technique is provided.
- Availability or equivalenceNames, formulations, units, and presentations can vary by market and over time.
Separate reference from record-keeping
Document the exact product and lot actually used
Aesthetic Pass records treatment identity, lot information, photos, and injection maps. The atlas itself never chooses a product or treatment.