What Goes Into Every OncoCare Product

And what we make sure never does

Our Commitment

Cancer patients deserve better than what the supplement industry typically offers

Most supplement brands are built around what sounds good on a label. OncoCare is built around what we would put in front of our own family member going through chemotherapy. That standard is different. It is more demanding. And it shows up in every sourcing decision we make.

cGMP Certified Facilities

Every OncoCare product is manufactured in FDA-registered facilities operating under current Good Manufacturing Practices (21 CFR Part 111). That means documented quality control at every step, from raw material testing to finished product release.

US-Based Manufacturing

We manufacture in the United States. Not because it is cheaper, it is not, but because US facilities operate under FDA oversight and are held to standards that protect our customers.

Third-Party Tested

Every lot is tested by independent third-party laboratories for identity, potency, heavy metals, and microbial contamination before it ships. We pursue NSF certification as an additional credibility layer for our oncology patient population.

We source the best available form of every ingredient. Not the cheapest.

In the supplement industry, the same ingredient can range from low-grade commodity powder to clinically validated, bioavailability-optimized branded forms. We always choose the form that the clinical research actually used.

IngredientPremium Form We UseWhy It Matters
MagnesiumAlbion TRAACS Bisglycinate ChelateChelated form absorbs significantly better than oxide or citrate forms commonly used in cheaper products
CoQ10Kaneka QH Ubiquinol (Japan)Reduced ubiquinol form; up to 8x more bioavailable than standard ubiquinone CoQ10
Vitamin K2MenaQ7 MK-7 All-Trans (Gnosis)All-trans configuration is the biologically active form; synthetic K2 often contains inactive cis isomers
SulforaphaneMyrosinase-Active Broccoli Sprout ExtractEnzyme-active form converts properly in the body; many products use inactive sulforaphane glucosinolate only
AHCCLicensed from Amino Up Co., JapanProprietary mushroom extract with the only published RCT in ovarian cancer patients; unlicensed AHCC copies lack verified molecular weight specifications
QuercetinQuercefit Phytosome (Indena, Italy)20x more bioavailable than standard quercetin aglycone used in most supplements
ZincAlbion TRAACS Bisglycinate ChelateChelated zinc absorbs 3-4x better than zinc oxide, the form used in most mass-market multivitamins

No fillers. No shortcuts. No compromises.

We are as rigorous about what we leave out as what we put in. The following have no place in supplements designed for cancer patients in active treatment.

Magnesium Stearate (flow agent filler)

A common manufacturing lubricant with no therapeutic value. We use cleaner alternatives.

Silicon Dioxide (anti-caking filler)

Another manufacturing convenience ingredient. Not in OncoCare.

Artificial Colors or Dyes

No FD&C dyes. No synthetic colorants of any kind.

Artificial Flavors or Sweeteners

No aspartame, sucralose, or synthetic flavor compounds.

Titanium Dioxide (whitening agent)

Increasingly flagged in safety literature. Excluded from all OncoCare products.

Carrageenan

Pro-inflammatory food additive common in capsule formulations. Excluded.

Gelatin Capsules

All OncoCare capsules use HPMC, a plant-derived shell. Suitable for all dietary preferences.

Proprietary Blends

We list every ingredient and every dose. No hidden blends. No underdosed label dressing.

Every lot. Every time.

We do not release a product until it passes independent third-party testing. Every batch is tested for:

Identity Verification

Confirms the ingredient is what the label says it is. Adulterants and substitutions are more common in the supplement industry than most consumers realize.

Potency Testing

Confirms that each ingredient is present at the dose stated on the label. Label claims must match what is actually in the capsule.

Heavy Metals

Tests for lead, mercury, arsenic, and cadmium per USP <232> standards. Critical for a patient population already managing significant physiological stress.

Microbial Contamination

Tests for harmful bacteria, yeast, and mold per USP <61> and <62>. Particularly important for immunocompromised patients on ADC therapy.

The standard we hold ourselves to is simple

Would we give this to Judy?

Every sourcing decision, every manufacturing requirement, every quality test comes back to that question. If the answer is not an immediate yes, we go back to the drawing board.