Quality & Transparency

Check what is in a Nutribota stick, match your lot to the finished-product report, and see which records cover the ingredient and manufacturing facility.

Start with what you want to check.

Each record answers a different question. The batch-specific results and document details are below.

For the current finished-product listing, visit the Nutribota Creatine Stick Packs product page. For the full topic map, visit Creatine Guides. The Creatine Hub connects current availability with related education.

Finished-Product Batch Testing: VB26097500

The provided SGS report image GZF26-0057291-01, dated September 24, 2026, identifies the submitted sample as Nutribota Creatine Monohydrate Stick Packs, batch VB26097500. The results below apply to that submitted sample and identified batch; they do not establish identical results for every stick or another batch.

  • Creatine monohydrate

    5.04 g/serving

    Amount measured for the submitted sample.

  • Heavy-metal tests

    Met report limits

    Lead, cadmium, arsenic and mercury.

  • Microbial testing

    Met specified limits

    For tests with limits shown in the report.

Match your product lot to this batch record

  1. Read the lot on your packaging. The finished-product record shown here identifies batch VB26097500. A different lot requires its own supporting record.
  2. Check the document identity. The provided SGS image identifies report GZF26-0057291-01, dated September 24, 2026, for the submitted Nutribota Creatine Monohydrate Stick Packs sample.
  3. Read the results with their units and comments. Expand the 12-result table below. Use the report image alongside the transcription; 5.04 g/serving is an amount for the submitted sample.

For a different lot or the complete original report, contact Nutribota with the product and lot details. The image on this page is the provided report image; a complete original PDF is not available for download here.

Sample and report details
  • Client: Pureblend Nutrition Inc.
  • Sample name: Creatine Monohydrate Stick Packs; brand: nutribota.
  • Batch number: VB26097500; production date: September 8, 2026.
  • Sample received: September 16, 2026; testing period: September 16–24, 2026.
  • Sample number / SGS sample ID: 0001 / GZF26-0057291-0001; description: Sample in bag.
  • Client-provided serving information: 5 g/day(serving). The report states that sample information was submitted and certified by the client.

Result highlights: the report lists 5.04 g of creatine monohydrate per serving, nine rows marked “Pass,” and three rows with a dash in the comment column. The 5.04 g/serving result is an analytical amount for the submitted sample, not a purity percentage or a guarantee of the amount in every stick. Follow the product label for serving directions.

Open the provided report image. This is an image of the provided report content, not a complete original PDF. The image does not show a signature, report-end statement or explanatory footnotes. For the complete original report or questions about a specific lot, contact Nutribota.

View all 12 reported results and the report image
Results transcribed from provided report image GZF26-0057291-01 for submitted sample 0001
Test item Reported result Result unit shown LOQ shown Limit shown Report comment Method reference
Total Aerobic Microbial Count 70 CFU/g — ≤10000 Pass Refer to USP-NF <61>, official date: 01-May-2025
Total Combined Molds and Yeasts Count <10 CFU/g — ≤1000 Pass Refer to USP-NF <2021>, official date: 01-Aug-2013
Mould <10 CFU/g — — — Refer to USP-NF <2021>, official date: 01-Aug-2013
Yeast <10 CFU/g — — — Refer to USP-NF <2021>, official date: 01-Aug-2013
Salmonella ND /10 g — Absence Pass Refer to USP-NF <2022>, official date: 01-Nov-2019
Staphylococcus aureus ND /10 g — Absence Pass Refer to USP-NF <2022>, official date: 01-Nov-2019
Escherichia Coli ND /10 g — Absence Pass Refer to USP-NF <2022>, official date: 01-Nov-2019
Lead (Pb) ND mg/day 0.05 mg/kg ≤0.005 Pass USP <233> elemental impurities—procedures, procedure 2
Cadmium (Cd) ND mg/day 0.005 mg/kg ≤0.005 Pass USP <233> elemental impurities—procedures, procedure 2
Arsenic (As) ND mg/day 0.005 mg/kg ≤0.015 Pass USP <233> elemental impurities—procedures, procedure 2
Mercury (Hg) ND mg/day 0.003 mg/kg ≤0.015 Pass USP <233> elemental impurities—procedures, procedure 2
Creatine monohydrate 5.04 g/serving 0.20% — — GB 24154-2015 Appendix B

“ND” is reproduced exactly as shown; it must not be read as zero. A dash means no value or comment is shown in that field. The microbial table has no LOQ column. For metals, the report lists the result unit and limits in mg/day but LOQ in mg/kg; these units are kept separate above. The creatine monohydrate row has no limit or Pass comment. Values, methods and reporting context should be read together with the original report.

SGS test report GZF26-0057291-01 dated September 24, 2026, for Nutribota Creatine Monohydrate Stick Packs, batch VB26097500
Provided report image: SGS GZF26-0057291-01, September 24, 2026; submitted sample identified as batch VB26097500. Open full-size image.

Document summary added October 3, 2026. Raw-material purity results and manufacturing facility certification are identified separately below.

GMP-Certified Manufacturing

Nutribota Creatine Monohydrate Stick Packs are manufactured in a facility certified by NSF to NSF/ANSI 455-2, Good Manufacturing Practices for Dietary Supplements.

GMP certification addresses the facility's manufacturing and quality-control systems. The certified scope includes powder products, mixing, and packaging/labeling operations.

What this certification covers: the manufacturing facility and its practices. It is separate from NSF product certification, NSF Certified for Sport®, and laboratory testing of a specific finished-product lot.

Learn about NSF's GMP certification program. For questions about a Nutribota product lot, contact our support team.

Watch: What Does GMP Mean When Buying Creatine?

This short Nutribota video explains the difference between manufacturing practices and finished-product testing.

Watch this GMP explanation on YouTube.

Key takeaway: GMP focuses on manufacturing practices. A facility certification and a laboratory report for an identified finished-product batch provide different information. Check the scope of each document.

Manufacturing certification reviewed September 30, 2026.

View the documents

Open the full-size images to read the ingredient documents in this section. They cover the licensing relationship and referenced raw material; they are not a finished-stick-pack COA. The separate provided report image for finished-product batch VB26097500 is identified above.

For context and document captions, see the Pürest ingredient document guide.

What Each Document Can Tell You

Record What it identifies What it does not establish
Provided finished-product report image: GZF26-0057291-01 The submitted stick-pack sample identified as batch VB26097500, with its reported results, units and limits. Product certification, identical results for every stick or another batch, or a finished-product purity percentage.
License & Supply Agreement excerpt The ingredient licensing and supply relationship described in the excerpt A laboratory test or finished-product certification.
Supplier COA: HPCM2026032301 The named raw material, specifications, reported results and footnotes That every listed item was freshly tested for every production batch.
Third-party report: CHG-50381416-0 The submitted sample, analytical results, method references and reporting limits Testing of a Nutribota finished stick-pack batch.
Manufacturing facility GMP certification The manufacturing facility's certification to NSF/ANSI 455-2, including powder and packaging operations NSF product certification, NSF Certified for Sport®, or a finished-stick-pack batch test.

The supplier COA notes that items marked with an asterisk are periodically analyzed and that triangle-marked data come from the third-party analytical report. Read these notes with the results. The analytical report also identifies its test-location code and detection and quantitation limits.

For a field-by-field explanation, read how to read the COA footnotes. For finished-product batch VB26097500, review the provided report image and batch-specific summary. For another lot or the complete original report, contact Nutribota with the product and lot details. The raw-material documents do not substitute for finished-product batch testing.

Pürest Creatine™ Ingredient Identity

Nutribota Creatine Monohydrate Stick Packs are a single-ingredient formula made with licensed Pürest Creatine™ creatine monohydrate. No fillers, blends, flavors, or additional active ingredients are added. Learn more in What Is Pürest Creatine™?.

Raw-Material Documentation

A referenced Certificate of Analysis for Pürest Creatine™ High Purity Creatine Monohydrate identifies batch HPCM2026032301, manufactured March 23, 2026, with a retest date of March 22, 2029.

For that referenced raw-material batch, the COA lists a dry-basis assay specification of at least 99.5% with a reported result of 100.2%, and a purity specification of at least 99.99% with a conforming result. A separate third-party analytical section for the same batch reports creatine purity of 99.999%.

Why the Raw-Material Result Matters

Because the Nutribota finished formula contains only Pürest Creatine™ creatine monohydrate and no added fillers or blends, the documented raw-material quality is directly relevant to the ingredient used to make the stick packs. We still identify the 99.999% result as a test result for the referenced Pürest Creatine™ raw-material batch rather than describing it as a separate finished-stick-pack purity test.

Impurities, Heavy Metals & Microbiology

The referenced documentation includes testing or specifications for creatinine, dicyandiamide, dihydrotriazine, cyanide, heavy metals, and microbiological indicators. The third-party analytical section reports dicyandiamide below 0.4 mg/kg, dihydrotriazine below 0.6 mg/kg, creatinine at 9.07 mg/kg, and unspecified impurity below 0.4 mg/kg.

The raw-material COA also lists results below the stated limits for lead, arsenic, cadmium, and mercury, along with microbiological results for total plate count, yeast and mold, E. coli, Salmonella, and S. aureus.

Raw-Material Testing and Finished-Product Testing

The referenced 99.999% result comes from third-party analysis of the identified Pürest Creatine™ raw-material batch. Nutribota does not relabel that document as a finished-product purity report. The provided finished-product report image for batch VB26097500 is identified separately so customers can see which submitted sample and batch each document covers.

How We Describe Testing

We avoid turning a single document into a broader claim than it supports. When Nutribota discusses a test result, the goal is to identify whether it refers to an ingredient, a specific batch, a third-party analysis, or a finished product.

Evidence Guides

Read the Creatine COA Guide to understand batch-specific certificates and the Creatine Purity Explained guide for purity terminology and evidence scope.

Official Reference

For a concise map of Nutribota’s current brand, flagship Creatine Stick Packs, Pürest Creatine™ relationship, and evidence boundaries, use the Nutribota Creatine Brand & Product Reference.

Document explanations updated October 4, 2026.

Learn More

For creatine basics, start with our Creatine Monohydrate Guide. For the ingredient-brand relationship, read What Is Pürest Creatine™?. For how Nutribota evaluates sources and separates current product facts from general education, see our Research & Editorial Standards.