Ingredient Dictionary/hydrolyzed-hyaluronic-acid/HYDROLYZED HYALURONIC ACID
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
Synthetic

HYDROLYZED HYALURONIC ACID

Hair ConditioningHumectantSkin Conditioning
[EU CosIng Official Definition] Hydrolyzed Hyaluronic Acid is the hydrolysate of Hyaluronic Acid derived by acid, enzyme or other method of hydrolysis
Executive Regulatory & Safety Fact BoxAEO / GEO CITATION ANCHOR

What is HYDROLYZED HYALURONIC ACID (CAS N/A) in cosmetics and what are its global regulatory limits?

HYDROLYZED HYALURONIC ACID (CAS No. N/A) is a verified cosmetic ingredient primarily functioning as Hair Conditioning, Humectant, Skin Conditioning in topical formulations. Regulated under KR MFDS (Unregulated) and EU 1223/2009 CosIng (Unregulated) statutory frameworks, it is typically formulated at 0.05–0.1% within an optimal stability window of pH 4–8.

7-Track Official Regulatory Label Names Matrix

Primary Statutory Gazette Only · Zero Machine Translation
7-Track Official Statutory Label Names for HYDROLYZED HYALURONIC ACID
Jurisdiction TrackOfficial Statutory Label NameOne-Click Copy
1. Korea (MFDS Standard Name)HYDROLYZED HYALURONIC ACID (KR MFDS Registered)
2. Korea Former Nomenclature History——
3. European Union (EU CosIng Glossary)HYDROLYZED HYALURONIC ACID
4. United States (US PCPC / MoCRA INCI)HYDROLYZED HYALURONIC ACID
5. US FDA OTC Monograph Active Name— (Cosmetic Inactive / Non-OTC)—
6. China (NMPA IECIC Standard Name)水解透明质酸
7. Japan (JCIA Standard / MHLW Quasi-Drug)加水分解ヒアルロン酸 · [QD: 加水分解ヒアルロン酸]

Layer 1 — Statutory Regulatory Limits Across 6 Regions

Layer 1 Statutory Regulatory Limits Across 6 Regions for HYDROLYZED HYALURONIC ACID
RegionStatusMax LimitConditions & Statutory Source
Korea (MFDS)UnregulatedGMPListed in official cosmetic inventory
Europe (EU)UnregulatedGMPListed in official cosmetic inventory
United States (FDA)UnregulatedGMPListed in official cosmetic inventory
China (NMPA)Listed / AllowedGMPIECIC Entry #6353
Japan (MHLW)UnregulatedGMPListed in official cosmetic inventory
ASEAN (ACD)UnregulatedGMPListed in official cosmetic inventory

Layer 2 — Toxicological & Historical Safe Use Concentrations (CIR / SCCS / CN IECIC / IFRA)

“EU SCCS Safe Opinion Limit” is the toxicological safe threshold (MoS≥100), whereas “US CIR Reported Max Use” and “CN IECIC Historical Max Use” represent historical maximum concentrations in commercial products.

Layer 2 Toxicological & Historical Safe Use Concentrations for HYDROLYZED HYALURONIC ACID
Assessment BasisApplication ScopeConcentration RangeVerdict & Dossier Reference
CN IECIC Historical Max Useleave_on≤ 2%Safe (MoS≥100)NMPA IECIC (2025) Entry 06154 (2025)
CN IECIC Historical Max Userinse_off≤ 1.5%Safe (MoS≥100)NMPA IECIC (2025) Entry 06154 (2025)
⚠️ Reference Only (Legal Disclaimer): The regulatory limits, ingredient names, and formulation ranges in this dictionary are provided for R&D reference only. Because official notices may be amended or data discrepancies may exist, users must verify the latest statutory text from the competent authority before product formulation, labeling, or commercialization. UNIZ LAB assumes no legal liability for the use of this information.
Interactive Quartile Box-Plot (Min–Q1–Median–Q3–Max)

Layer 3 Formulation Concentration Box-Plot vs. Statutory Limit

Aqueous Serum / Ampoulen=6
Min 0.05% · Q1 0.0625% · Median 0.1% · Q3 0.1% · Max 0.1%
Emulsion / Creamn=17
Min 0.03% · Q1 0.1% · Median 0.1% · Q3 0.1% · Max 0.5%
Aqueous Serum / Ampoule — Aqueous serum, toner & hydrogel matrix formulation component
Verified Source: Global Starter Formulation Library Statistical Distribution (n=6, EVONIK 6) (cir_safety) · EVONIK 6
Typical Median: 0.1%

Layer 3 — Formulation Usage Guide (Quartiles n≥5) & Physicochemical Compatibility

Layer 3 Formulation Concentration Quartiles by Product Category for HYDROLYZED HYALURONIC ACID
Formulation GroupMin – Q1 – Median – Q3 – Max (%)Role & MechanismSource ID
Group A — Aqueous Toner / Serum / Ampoule0.05% · 0.0625% · 0.1% · 0.1% · 0.1%Aqueous serum, toner & hydrogel matrix formulation componentGlobal Starter Formulation Library Statistical Distribution (n=6, EVONIK 6)
Group B — O/W & W/O Emulsion / Lotion / Cream0.03% · 0.1% · 0.1% · 0.1% · 0.5%Emulsion cream & lotion structural / conditioning agentGlobal Starter Formulation Library Statistical Distribution (n=17, EVONIK 17)
Cutaneous Permeation Science (500 Dalton Rule)MW: Macro/Complex · LogP: N/A

Stratum Corneum Penetration Depth & Bio-Spicule Transdermal Delivery

Stratum Corneum (Brick & Mortar Barrier · 10–20 µm)500 Da Molecular Weight Cutoff BarrierViable Epidermis (Keratinocytes & Melanocytes · 50–100 µm)Target for Brightening (Tyrosinase/Melanosome) & Barrier LipidsPapillary Dermis (Fibroblasts & ECM Collagen · 150–300 µm)Target for Collagen I/III Synthesis, Peptides, PDRN & ExosomesEpidermal Passive Permeation (<500 Da)
Molecular Weight & LogP Permeation Diagnosis
Low Molecular Weight (320 Da ≤ 500 Da) — Passive Permeation Feasible

Under passive topical application, molecules diffuse tortuously through intercellular lipids. Hydrophilic compounds >500 Da remain primarily on the outer stratum corneum.

Estimated Target Depth
40–90 µm
Optimal Delivery System
Polyol Enhancer / Serum
Colloid Interface, pH Spectrum & Thermal Stability

pH Stability Window (0–14), Thermal Limit & HLB Colloidal Phase Behavior

Water or glycol phase soluble/dispersible
Optimal Formulation pH Stability Window (0–14)pH 4.0 – 8.0
0245.5791114

Outside pH 4–8, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 50°C
25°C45°C60°C75°C85°C100°C

Thermally stable up to 50°C during standard emulsification.

HLB Scale (0–20) & Colloidal Micelle / Lamellar Phase Simulator
O/W Oil-in-Water Micelle Emulsion (Lotion / Cream)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
Biochemical Signaling & Mechanism Pathway

Cellular & Molecular Target Mechanism Flow

1. Epidermal Interaction→ Upregulation / Activation
Intercellular Lipid & Hydration Matrix
→
TEWL Reduction & Barrier Conditioning
2. Homeostasis Modulation⊣ Inhibition / Blockade
Oxidative Stress (ROS) & Irritant Cascade
⊣
Cutaneous Soothing & Homeostasis
Formulation Ontology Radial Graph

Interactive Synergy Pairings (Solid) & Incompatibility Warnings (Dashed)

+ GLYCERIN+ CAPRYLIC/CAPRIC TR…+ TOCOPHEROL✕ Verify phase compati…HYDROLYZED HYALURO…
Interactive Node Guide

Click any green synergy node to jump directly to its monograph, or click a red dashed node to inspect the chemical incompatibility mechanism.

Nominative Trade Name References (Trademark Act Art. 90(1)(2))
HYDROLYZED HYALURONIC ACID

Trade names are provided strictly for descriptive identification of polymer/emulsifier grades under Article 90(1)(2) of the Trademark Act. All trademarks belong to their respective owners.

Academic & Toxicological Synthesis

Tier 1 Synthesis

Synthesized strictly from peer-reviewed PubMed abstracts and official toxicological dossiers linked to this ingredient.

■ [1. Chemical Identity & International Labeling Nomenclature] - INCI Name: HYDROLYZED HYALURONIC ACID | CAS No.: N/A | EC No.: N/A - Origin: SYNTHETIC | Functions: , , - Physicochemical Profile: Formula | MW /(Polymer/Complex) | / | Ionic Nature: non-ionic | CosIng/MFDS - Official Regional Label Names: US [HYDROLYZED HYALURONIC ACID] · EU [HYDROLYZED HYALURONIC ACID] · CN [水解透明质酸] · JP [加水分解ヒアルロン酸] · JP Quasi-Drug [加水分解ヒアルロン酸] ■ [2. Dermatological Mechanism of Action & Functional Role] - Hydrolyzed Hyaluronic Acid is the hydrolysate of Hyaluronic Acid derived by acid, enzyme or other method of hydrolysis Classified under origin 'synthetic', it acts within the cosmetic vehicle or stratum corneum to deliver , , performance and structural formulation stability. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: NONE | EU: NONE | US: NONE | CN: ALLOWED | JP: NONE | ASEAN: NONE (CN IECIC (2025) Entry No. 6353 (水解透明质酸)) - No specific Annex prohibition or numeric restriction across the 6 major jurisdictions (Permitted under general GMP safety assessment). - Official Safety & Historical Use Concentration (Layer 2): CN_IECIC_2025 (cn_iecic_max, leave_on): Max 2.0% / CN_IECIC_2025 (cn_iecic_max, rinse_off): Max 1.5% ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [aqueous_serum] Typical range: 0.05 ~ 0.1% (Median 0.1%, Ref: Global Starter Formulation Library Statistical Distribution (n=6, EVONIK 6)) — Aqueous serum, toner & hydrogel matrix formulation component - [emulsion_cream] Typical range: 0.03 ~ 0.5% (Median 0.1%, Ref: Global Starter Formulation Library Statistical Distribution (n=17, EVONIK 17)) — Emulsion cream & lotion structural / conditioning agent ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Water Phase or Cool-down Phase (< 45°C) - Optimal pH Range: pH 4.0 ~ 8.0 | Max Process Temp: Max 50°C | Electrolyte Tolerance: MEDIUM - Incompatibility / Caution: Verify phase compatibility under extreme pH or high electrolyte loads - Synergy Pairings: GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL | Reference Trade Names: HYDROLYZED HYALURONIC ACID ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 36547309 (2022, Gels): Fabrication of High-Resolution Fine Microneedles Derived from Hydrolyzed Hyaluronic Acid Gels in Vacuum Environment Impr - PMID 31376454 (2019, Int J Biol Macromol): Various methods to combine hyaluronic acid and antimicrobial peptides coatings and evaluation of their antibacterial beh - PMID 13076197 (1953, Science): Inactivation of vaccinia virus by a diffusible component from hydrolyzed hyaluronic acid

Linked Peer-Reviewed Literature (NIH PubMed) (3)

Fabrication of High-Resolution Fine Microneedles Derived from Hydrolyzed Hyaluronic Acid Gels in Vacuum Environment Imprinting Using Water Permeable Mold [PMID: 36547309 · 2022]
Miura S, Yamagishi R, Miyazaki R, Yasuda K, Kawano Y, Yokoyama Y, Sugino N, Kameda T, Takei S · Gels (2022)

Hydrolyzed hyaluronic acid high-resolution fine microneedles of 13 &#xb5;m in diameter and 24 &#xb5;m in height were fabricated from hydrolyzed hyaluronic acid gels made in mixtures of water using vacuum environment imprint lithography processes with a water permeable mold. The gas traps of water and volatile solvents in the imprint materials cause transfer failure in the conventional water impermeable molds of quartz and metal. However, the water permeable mold allows the use of 67 wt% dilution water with high solubility to increase the fluidity of the hydrolyzed hyaluronic acid during the patterning of high-resolution fine microneedles for cosmetics and pharmaceuticals. This demonstration sets a new paradigm of functional pure gels for high-resolution nano-patterning applications with various cosmetic and pharmaceutical materials containing dilution water using a water permeable mold.

Various methods to combine hyaluronic acid and antimicrobial peptides coatings and evaluation of their antibacterial behaviour [PMID: 31376454 · 2019]
Paris JB, Seyer D, Jouenne T, Th&#xe9;bault P · Int J Biol Macromol (2019)

To prevent bacterial adhesion and contamination, biomaterials exhibiting both antiadhesive and biocidal properties are the most promising way. However, control of the properties combination is not so easy due, in particular, to antagonist mechanisms. Antibacterial surfaces against Staphylococcus epidermidis adhesion were here elaborated by using both nisin grafting and repelling polysaccharide coating. We evaluated two strategies aiming to improve the antimicrobial peptide (AMP) immobilization parameters (i.e., the accessibility and/or local density) in order to obtain the best antimicrobial activity on surfaces. We thus (i) grafted the nisin on a surface previously coated with hydrolyzed hyaluronic acid (HA) (to decrease the length of the polysaccharide chains) or (ii) coupled nisin and HA in solution before grafting this complex on surfaces. XPS analysis pointed out a lower amount of nisin on the surface for both approaches compared to the immobilization of nisin on native HA. However, an antibacterial activity was maintained, probably due to a higher local density of the AMP when surfaces were modified with hydrolyzed hyaluronic acid, leading to a better combination of antiadhesive-biocidal properties. Microscopy fluorescent observations demonstrated that accumulation of dead cells was also avoided by some coatings architecture.

Inactivation of vaccinia virus by a diffusible component from hydrolyzed hyaluronic acid [PMID: 13076197 · 1953]
MCCREA JF, DURAN-REYNALS F · Science (1953)

Frequently Asked Questions (AEO Position 0)

Q1. What are the official 7-track regulatory label names for HYDROLYZED HYALURONIC ACID?
Standard label names are US PCPC INCI: 'HYDROLYZED HYALURONIC ACID', EU CosIng: 'HYDROLYZED HYALURONIC ACID', KR MFDS: 'HYDROLYZED HYALURONIC ACID (KR MFDS Registered)', CN NMPA IECIC: '水解透明质酸', and JP JCIA: '加水分解ヒアルロン酸'.
Q2. Is HYDROLYZED HYALURONIC ACID restricted or permitted in EU, US, KR, CN, and JP cosmetics?
Regulatory status summary across 6 jurisdictions — KR: none, EU: none, US: none, CN: allowed, JP: none, ASEAN: none.
Q3. What is the typical formulation concentration and optimal pH window for HYDROLYZED HYALURONIC ACID?
In aqueous_serum systems, HYDROLYZED HYALURONIC ACID is typically formulated between 0.05% and 0.1% (median 0.1%), with an optimal stability window of pH 4–8.
Q4. What are the known formulation incompatibilities and synergy pairings for HYDROLYZED HYALURONIC ACID?
Recommended synergy pairings include GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL. Key incompatibilities to avoid: Verify phase compatibility under extreme pH or high electrolyte loads.