Quality Standards
Age Revive's quality approach is built on five pillars: full-dose disclosure (every ingredient amount printed on the label, no proprietary blends), identity verification confirming each raw material matches its label claim, potency verification on the finished product to ensure labeled doses are delivered, contaminant screening aligned to each ingredient's risk profile, and lot-level traceability with batch records available on request. All products are manufactured in cGMP-compliant facilities in the United States. This page explains each pillar in detail and provides the quality checklist Age Revive applies to every formula.
Reviewed by Andy Palenzuela, Founder. Last updated 2026-09-22. The current CELLUBIOME lot certificate is published below. Certificates for other lots are available on request — email support@agerevive.com with the lot number printed on the bottle.
Quality overview
- Identity and potency verification for finished product
- Contaminant screening categories aligned to ingredient risk profile
- Lot-level traceability and documentation support
- Delivery integrity validation for targeted release formats
Simple buyer audit checklist
Start with how to read a certificate.
- Is the full dose disclosed for each core active (no proprietary blend)?
- Is there identity verification for each lot?
- Is there potency verification for the finished product?
- Is there contaminant screening appropriate to ingredient risk profile?
- Is there traceability with lot numbers and batch records?
- If delivery claims exist, is delivery integrity validated?
Testing standards
| Category | What it checks | Why it matters |
|---|---|---|
| Identity | Confirms ingredient matches label claim. | Prevents substitution and sourcing errors. |
| Potency | Confirms labeled actives are present at labeled dose. | Dose connects research and product output. |
| Heavy metals | Screens for lead, arsenic, cadmium, mercury. | Reduces avoidable exposure risk. |
| Microbiological | Screens for microbial contamination. | Protects production and storage quality. |
| Residual solvents | Screens extraction-related residues where relevant. | Supports extraction quality control. |
| Format integrity | Checks delivery integrity where enteric or targeted release is used. | Delivery claims require verification. |
Current lot certificates
Every lot is third-party tested for identity and potency. Results publish here as each certificate is issued.
CELLUBIOME — Lot 150126
Tested by Delta Labs of South Florida Corp., an ISO/IEC 17025:2017-accredited laboratory.
| Test | Result | Label claim |
|---|---|---|
| Urolithin A, per 2 capsules | 548.15 mg | Not less than 500 mg |
| Tributyrin, per 2 capsules | 530.80 mg | Not less than 500 mg |
| Microbial panel | Passed | — |
| Staphylococcus aureus | Negative | — |
| Heavy metals | Screened by ICP-MS | — |
Certificate PDF pending upload.
CELLUNAD+ — current lot
Certificate in progress. It publishes here when issued. No CELLUNAD+ tested values are stated until then.
CELLUNOVA
Not currently in production. Certificate publishes with the next production run.
How to read a certificate of analysis
A certificate of analysis (CoA) is the document behind the phrase "third-party tested." Five things to look for on any brand's certificate, including ours:
- The laboratory's name and accreditation. ISO/IEC 17025 is the international standard for testing laboratories. A certificate from an unnamed lab, or from the manufacturer's own bench, is a different document.
- The lot number — and that it matches your bottle. A certificate for a lot you did not receive tells you about a batch you do not own.
- The tested value next to the label claim. "Not less than 500 mg" on the label and 548.15 mg on the certificate is a pass. A certificate that shows only "conforms" without a number is asking for trust it has not earned.
- What was screened, not just what passed. Identity, potency, microbial, heavy metals — and for extraction-based ingredients, residual solvents. The panel should match the ingredient's risk profile.
- The date. Certificates are per-lot. A three-year-old certificate is a historical document.
The founder of Age Revive spent 14+ years inside regulated nutrition supply chains, including quality assurance. The short version of that experience: "third-party tested" is a claim, a certificate is evidence, and the two are not the same thing.
Manufacturing and compliance
- cGMP manufacturing is baseline, not a premium signal by itself.
- Supplier qualification is required because raw material variability exists.
- Release criteria should tie to identity, potency, and contaminant thresholds.
- For longevity protocols, consistency across lots matters as much as mechanism selection.
Traceability and documentation
- Lot numbers should be printed on bottles.
- Batch records should tie raw material and finished product checks to each lot.
- Documentation requests should include product name and lot number.
Label transparency
- No proprietary blends.
- Core actives and doses are disclosed so research comparisons are possible.
- Known allergens are disclosed on-label (CELLUNOVA contains wheat).
Glass, not plastic
Age Revive bottles in glass. Glass does not leach, does not absorb odor, and does not interact with oily actives like tributyrin. It is heavier and costs more to ship. That is a standard we chose, not a health claim.
Product-specific notes
- CELLUNAD+: Daily NAD+ pathway support where consistency and dose transparency are critical. See every study, with what it did and did not show.
- CELLUBIOME: Gut and mitochondrial support where enteric delivery integrity is part of design intent. See every study, with what it did and did not show.
- CELLUNOVA: 7-day protocol where batch controls and allergen disclosure are important.
Quality FAQ
- What does third-party tested mean here?
- It means independent testing is used to verify identity and potency and to screen for common contaminants. Exact panels can vary by ingredient and risk profile. For CELLUBIOME, the current lot certificate with tested values is published on this page.
- Do you provide Certificates of Analysis (CoAs)?
- Yes. The current CELLUBIOME certificate is published above. Certificates for other lots are available on request: email support@agerevive.com with the product name and the lot number printed on the bottle.
- Is Age Revive GMP-certified, NSF-certified, or organic?
- Age Revive products are manufactured in cGMP-compliant facilities in the United States. We do not claim NSF, Informed-Sport, organic, non-GMO, gluten-free, vegan, or kosher certification, because none of those has been established for these products. We state what we can show.
- Do you use proprietary blends?
- No. Proprietary blends hide doses and prevent meaningful evaluation. Age Revive discloses core actives and doses so the product can be audited.
- What contaminants do you screen for?
- Common screening categories include identity verification, potency, heavy metals, and microbiological contaminants. Additional panels may apply based on ingredient sourcing and extraction methods.
- How do you handle allergens?
- Known allergens should be disclosed on-label. CELLUNOVA contains wheat (spermidine source). If you have allergies or sensitivities, review Supplement Facts and consult a clinician if needed.
- How do I find my lot number?
- Lot numbers are printed on the bottle, often near the label edge or on the bottom. Use that lot number when requesting documentation so the correct records are pulled.
- Is this page medical advice?
- No. This page explains manufacturing and quality concepts. Products are dietary supplements and are not intended to diagnose, treat, cure, or prevent any disease.
Who we are: About Age Revive · Is Age Revive legit?