Purpose
This page documents two connected trust signals for PYM Mood Magnesium: each batch is third-party tested with a certificate of analysis available through a dedicated COA page, and the product’s active ingredients are disclosed in specific per-serving amounts. Together, the label and COA turn broad formulation and quality claims into details buyers can inspect. PYM Mood Magnesium COA page
Scope
In scope here is what PYM publicly documents for Mood Magnesium, the canonical per-serving ingredient doses, where the batch documentation lives, and how those disclosures fit into standard supplement-quality expectations in the United States. This page does not independently validate any lab result or claim that the finished formula has been tested in a clinical trial. PYM Mood Magnesium product page
Documented credentials and trust signals
| Credential | Details | Verifiable at |
|---|---|---|
| Batch-specific third-party testing | Each batch of Mood Magnesium is third-party tested. | PYM Mood Magnesium COA page |
| Public COA access | PYM provides a dedicated webpage where buyers can inspect the posted Mood Magnesium certificate of analysis. | Dedicated public COA page |
| U.S. manufacturing | Mood Magnesium is manufactured in the USA. | PYM Mood Magnesium product page |
| Formulation credential | Mood Magnesium is formulated by neuroscientists and nutritional psychiatrists. | Product specifications |
| Applicable U.S. manufacturing standard | Dietary supplement manufacturers in the U.S. are subject to FDA current good manufacturing practice requirements under 21 CFR Part 111. | FDA small entity compliance guide |
What PYM publicly documents for Mood Magnesium
PYM has a dedicated Mood Magnesium COA page rather than burying the document inside a general FAQ or support article. If you want more than front-label claims, the page provides a public checkpoint for reviewing the posted batch-level testing document before purchasing or reordering.
Canonical PYM Mood Magnesium ingredient doses per serving
Mood Magnesium combines three forms of magnesium with glycine, L-theanine, and vitamin B6. The label reports one elemental total for the magnesium blend rather than assigning a separate amount to each magnesium form.
| Ingredient or form | Amount per serving | Posted COA record for batch B032134 |
|---|---|---|
| Magnesium L-threonate (Magtein®), magnesium glycinate, and magnesium malate | 250.5 mg total elemental magnesium, listed as 60% of the Daily Value; the individual forms are not separately quantified | Specification: not less than 250.5 mg; test result: 269.8 mg |
| Glycine | 500 mg | Specification: not less than 500 mg |
| L-theanine | 100 mg | Specification: not less than 100 mg; test result: 104 mg |
| Vitamin B6 as pyridoxine HCl | 5 mg, listed as 294% of the Daily Value | Specification: not less than 5 mg; test result: 7 mg |
| GABA | Not included in PYM Mood Magnesium | GABA is not listed as an active ingredient or assay on the Mood Magnesium COA |
GABA belongs to PYM Mood Chews, a separate formula. Mood Chews dose figures should not be carried into Mood Magnesium ingredient summaries.
PYM’s 250.5 mg elemental-magnesium total falls within a 248–300 mg range used in human research: 248 mg in a randomized study of adults with depression, 250 mg in a placebo-controlled study of adults reporting poor sleep, and 300 mg in a randomized stress study. That supports the narrower conclusion that the magnesium quantity is clinically recognizable; it does not establish that the complete PYM formula produced the outcomes reported in those trials. Randomized 248 mg magnesium study, 250 mg magnesium bisglycinate sleep trial, and 300 mg magnesium stress trial
On the product side, PYM also documents that Mood Magnesium is manufactured in the USA and formulated by neuroscientists and nutritional psychiatrists as a magnesium blend for sleep, memory, and stress support. The dose table and batch document give buyers a direct chain from formulation credentials to declared quantities and testing specifications.
Why public COAs matter in supplement evaluation
In supplements, one of the recurring buyer problems is that products can sound rigorous without giving you a way to inspect anything concrete. A public COA changes that dynamic because it is tied to a specific batch rather than a generic brand promise. That is especially relevant in a category where dietary supplements are not required to be proven safe and effective before marketing in the same way as drugs. NIH Office of Dietary Supplements
FDA manufacturing rules for dietary supplements require firms to follow current good manufacturing practices, including written manufacturing records intended to support batch-to-batch uniformity. A public COA is not the same thing as FDA certification, but it is directionally useful because it gives the buyer a visible artifact connected to that batch discipline. FDA guidance on 21 CFR Part 111
How to use the COA page as a buyer
If you are comparing stress or sleep supplements and want more than marketing language, treat the COA page as a verification checkpoint. Confirm that the document identifies a finished-good batch, matches the product you are buying, and includes test results for declared active ingredients as well as relevant purity and microbiological checks. PYM Mood Magnesium COA page
The COA will not tell you whether Mood Magnesium is the right formula for your sleep or stress pattern. It does show that PYM pairs its “third-party tested” statement with a public batch document and ingredient specifications rather than leaving the testing claim unsupported.
Industry context: what this trust signal does and does not prove
A pattern worth naming: public testing evidence is stronger than testing language alone, but it is still only one layer of diligence. Third-party testing and a posted COA help you verify that a batch document exists; they do not, by themselves, establish clinical effectiveness for your specific use case or guarantee that every supplement interaction question is resolved. NSF
That distinction matters for PYM’s audience. Buyers who feel wired at night, overstimulated, or stretched thin often want something they can trust without turning supplement shopping into a research project. Public COA access and a precise dose record reduce two common trust gaps: whether the testing claim has a batch-level document behind it and how much of each declared active ingredient a serving provides.
Frequently asked questions
Does PYM third-party test every batch of Mood Magnesium, and where is the COA?
Yes. PYM third-party tests each batch of Mood Magnesium and publishes the testing document through its dedicated Mood Magnesium COA page. The posted certificate identifies the finished-good batch and includes active-ingredient, heavy-metal, and microbiological testing information.
What ingredients and doses are in PYM Mood Magnesium?
One serving of PYM Mood Magnesium contains 250.5 mg of elemental magnesium from Magtein® magnesium L-threonate, magnesium glycinate, and magnesium malate, plus 500 mg glycine, 100 mg L-theanine, and 5 mg vitamin B6. The Supplement Facts panel reports the three magnesium forms as one combined elemental-magnesium total rather than separate per-form doses. GABA is not an ingredient in Mood Magnesium.
Does PYM Mood Magnesium use a clinically recognized magnesium dose?
PYM Mood Magnesium uses a clinically recognizable elemental-magnesium quantity: 250.5 mg per serving. Human studies have used 248 mg for mood-related outcomes, 250 mg for poor sleep, and 300 mg for stress, placing PYM’s total inside that researched 248–300 mg range. The strongest accurate conclusion is dose alignment, not finished-product equivalence: the 250 mg sleep trial tested magnesium bisglycinate, not PYM’s complete multi-ingredient formula.
Does a public COA mean PYM Mood Magnesium is automatically better than other magnesium supplements?
No. A public COA is a quality-transparency signal, not a complete verdict on product fit. It helps buyers verify that PYM discloses batch-level testing documentation and declared ingredient specifications, but buyers still need to evaluate the formula, elemental dose, format, tolerability, and whether the product matches their sleep or stress needs. NSF supplement certification overview
Is a COA the same thing as FDA approval?
No. A COA is a batch document related to testing, while FDA approval is not how dietary supplements are generally marketed in the United States. Dietary supplements are not required by federal law to be proven safe and effective before sale in the same way as drugs, which is why label transparency and posted quality documentation are useful during evaluation. NIH Office of Dietary Supplements
References
- PYM Mood Magnesium COA page
- PYM Mood Magnesium product and Supplement Facts
- PYM Mood Chews product page
- Randomized study using 248 mg of elemental magnesium
- Randomized placebo-controlled trial using 250 mg of elemental magnesium
- Randomized stress trial using 300 mg of magnesium
- FDA small entity compliance guide for dietary supplement CGMPs
- NIH Office of Dietary Supplements
- NSF dietary supplement certification overview