AURA+
Skin & Tissue Support
GHK-Cu
Peptide Complex · 50 mg · 5 mL
This page provides general product information and handling guidance for AURA+ GHK-Cu 50 mg Peptide Complex. Reconstitution and use should be performed only under the direction of a qualified healthcare professional and in accordance with the applicable professional protocol.
about the product
AURA+ GHK-Cu is a lyophilized copper peptide formulation containing 50 mg of Copper Tripeptide-1 and supplied with 5 mL of diluent.
GHK-Cu is a naturally occurring copper-binding tripeptide studied for its role in cellular signaling, collagen regulation, extracellular matrix remodeling and skin repair. Within the ORCHESTRA portfolio, AURA+ GHK-Cu focuses on professional regenerative and aesthetic applications related to skin vitality, texture and tissue support.
What’s Included
- One vial of lyophilized Copper Tripeptide-1 — 50 mg.
- One vial of supplied diluent — 5 mL.
- One dropper, supplied separately.
product overview
- Product Name: AURA+ GHK-Cu Peptide Complex.
- ORCHESTRA Line: AURA+.
- Product Type: Lyophilized Copper Peptide Complex.
- Active Peptide: Copper Tripeptide-1.
- Peptide Complex: GHK-Cu.
- Format: Lyophilized Component with Supplied Diluent.
- Lyophilized Content: 50 mg.
- Diluent Volume: 5 mL.
- Final Volume After Reconstitution: 5 mL.
- Nominal Final Concentration: 10 mg/mL.
- Intended Setting: Professional Use.
Ingredients
- Lyophilized Component: Copper Tripeptide-1, 50 mg.
- Diluent: Water, Glycerin, 1,2-Propanediol, Phenoxyethanol and Caprylyl Glycol.
Storage Before Reconstitution
- Store at controlled room temperature.
- Do not freeze.
- Protect from light.
- Keep both vials sealed in their original packaging until use.
- Avoid excessive heat and temperature fluctuations.
- Keep out of reach of children.
Reconstitution Information
- Reconstitution must be performed by a qualified healthcare professional using aseptic technique and appropriate sterile transfer equipment suitable for sealed vials.
- Use only the supplied 5 mL diluent.
- Prepare a clean and sanitized work surface before handling the product.
- Inspect the lyophilized vial and supplied diluent vial before use.
- Do not use either vial if its protective seal is broken or damaged, or if its contents appear compromised.
- Remove the protective caps to expose the vial stoppers without removing or damaging the aluminum seals.
- Clean both vial stoppers with a sterile alcohol swab and allow them to air-dry completely.
- Using a new sterile syringe and sterile transfer needle, withdraw the complete 5 mL volume of supplied diluent.
- Slowly transfer the supplied diluent into the lyophilized vial.
- Direct the diluent gently against the inner wall of the vial where possible to minimize foaming and unnecessary agitation.
- Remove the syringe and needle after the complete diluent volume has been transferred.
- Dispose of the used syringe and needle in an approved sharps container.
- Gently swirl or roll the vial until the lyophilized component is fully dissolved.
- Do not shake the vial vigorously.
- Allow the solution to settle and inspect it carefully before use.
- Do not use the reconstituted product if visible contamination, abnormal discoloration, persistent cloudiness or unexpected particles are observed.
- After reconstitution, the final volume is 5 mL.
- After reconstitution, the nominal final concentration is 10 mg/mL.
- The appropriate route of use, quantity, frequency and application method must be determined by the qualified healthcare professional responsible for the protocol.
- The supplied dropper should be used only when appropriate to the selected professional protocol.
Storage After Reconstitution
- Post-reconstitution handling, storage conditions and the maximum in-use period must be determined by the qualified healthcare professional responsible for the protocol.
- Use the reconstituted product promptly whenever possible.
- If the complete volume is not used immediately, retain or reuse the remaining product only under storage conditions established for the applicable professional protocol.
- Keep the reconstituted product securely closed and protected from light.
- Do not freeze.
- Avoid unnecessary or prolonged exposure to heat.
- Do not use if the solution develops abnormal discoloration, persistent cloudiness, visible contamination or unexpected particles.
- Discard any remaining product when directed by the qualified healthcare professional responsible for the protocol.
warnings
- For professional use only.
- Reconstitution and use must be performed under the direction of a qualified healthcare professional.
- The route of administration or application, quantity, frequency and duration of use must be determined by the qualified healthcare professional responsible for the protocol.
- This page provides general product information and does not replace product-specific professional guidance.
- Use only the supplied diluent.
- Do not use if the packaging, vial or protective seal is broken or damaged.
- Do not use if the product appears contaminated or otherwise compromised.
- Do not use after the expiration date shown on the packaging.
- Do not use if an unexpected change in appearance is observed after reconstitution.
- Do not freeze.
- Keep out of reach of children.
Manufacturing & Origin
- Manufacturer: ProStemEx, LLC.
- Country of Manufacture: United States.
- Brand: ORCHESTRA.
Batch & Expiration
- Lot Number: See packaging.
- Expiration Date: See packaging.
Documentation
- For additional product documentation, batch-specific information or available quality and compliance documentation, contact ORCHESTRA.