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 April 2026. The current CELLUBIOME Certificate of Analysis is published at /quality/cellubiome/coa. Questions: 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
- 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. |
TESTING & CERTIFICATES
FINISHED-PRODUCT TESTING, LOT BY LOT.
Every lot is tested by an ISO/IEC 17025:2017-accredited independent laboratory. Results below are from finished-product testing of the current lot.
CELLUBIOME — Lot 150126
Sample received: 01/14/26 · Lab ID 22388
Analytical/Chemical Certificate of Analysis (finished product) · Delta Labs of South Florida Corp. · ISO/IEC 17025:2017 — PJLA Accreditation # 114871
| Test | Method | Reported result | Specification | Status |
|---|---|---|---|---|
| Assay Urolithin A | Urolithin A via HPLC | 548.15 mg/2 capsules | NLT 500 mg/2 capsules | Meets specification |
| Assay Tributyrin | Tributyrin via GC | 530.80 mg/2 capsules | NLT 500 mg/2 capsules | Meets specification |
| Lead (Pb) | Heavy Metals via ICP-MS | 0.0540 mcg/serving | Report Results in mcg/serving | Reported |
| Arsenic (As) | Heavy Metals via ICP-MS | 0.0414 mcg/serving | Report Results in mcg/serving | Reported |
| Mercury (Hg) | Heavy Metals via ICP-MS | 0.0000 mcg/serving | Report Results in mcg/serving | Reported |
| Cadmium (Cd) | Heavy Metals via ICP-MS | 0.0547 mcg/serving | Report Results in mcg/serving | Reported |
| Chromium | Chromium via ICP-MS | 1.40 mcg/serving | Report Result | Reported |
| Total Plate Count | USP 43 <61> | 100 CFU/g | NMT 10,000 CFU/g | Meets specification |
| Total Yeast and Mold | USP 43 <62> | 60 CFU/g | NMT 1,000 CFU/g | Meets specification |
| Staphylococcus aureus | USP 43 <61>/<62> | Negative | Negative | Meets specification |
View the CELLUBIOME quality-evidence page →
CELLUNAD+ — current-lot certificate in progress; results publish here on receipt.
The full certificate transcription and original report image are published at /quality/cellubiome/coa. Questions: support@agerevive.com with your lot number.
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).
Product-specific notes
- CELLUNAD+: Daily NAD+ pathway support where consistency and dose transparency are critical.
- CELLUBIOME: Gut and mitochondrial support where enteric delivery integrity is part of design intent.
- 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.
- Do you provide Certificates of Analysis (CoAs)?
- Yes — the current CELLUBIOME lot's third-party results are published in the Testing & Certificates section on this page, and the certificate is displayed on the product page. Full certificate PDFs publish here upon the lab's written release. You can also request a copy anytime at support@agerevive.com with your lot number.
- 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.