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COA explainer · United States

South Dakota: from grow to shelf, what the label has to show

Play it: a batch moves through South Dakota’s medical cannabis program on the left, and each required label piece snaps onto the package on the right, color-coded by who adds it.

Sample data · South Dakota (Department of Health, ARSD 44:90; SDCL 34-20G, medical program) · for illustration

🏷️ The product label, building live

Pasque Kitchen · Prairie Berry Gummies
Medical cannabis edible, 10 pieces
Fictional sample label for illustration, not a compliant, printable label.
🌱 Cultivation facility adds it🏭 Manufacturer adds it🔬 Testing facility / COA adds it🏛️ Department of Health (always required)
The big idea: South Dakota is medical only, and the Department of Health runs the whole program. The testing facility or its trained designee pulls every sample, every batch is tested in final form for potency and five contaminant groups before it can move, and results reach Metrc by midnight. A batch that fails for metals or pesticides can never be remediated, and edibles wear the Department’s yellow triangle with a leaf.

Sample label for illustration, not a compliant, printable label. South Dakota rules (Department of Health, ARSD 44:90; SDCL 34-20G), current October 2026. Educational, not legal advice.

Step by step: South Dakota

  1. Step 1: One strain, one harvest, 50 lb max (Cultivation facility) A cultivation facility registered with the South Dakota Department of Health splits its flower into homogenous batches of 50 pounds or less, each from one strain and one harvest date; a bigger harvest is divided before sampling. Each batch gets a unique batch identifier, tracked in Metrc, the state’s seed-to-sale system.
  2. Step 2: Manufacturer makes the edible (Manufacturer) A licensed manufacturer turns the flower into gummies, in batches of no more than 70,000 servings. An edible may hold no more than 50 mg of THC per serving and 500 mg per package, and its label gives the serving size and number of servings. Since 1 October 2025 it also carries an expiration date no more than 12 months after manufacture.
  3. Step 3: The lab’s designee pulls the sample (Testing facility) State law says a sample must be collected by a designated representative of the testing facility, a person or entity the lab authorizes in writing. A designee needs at least five hours of initial training and three hours a year after that. The batch is checked and homogenized first, and while results are pending its storage container is labeled PRODUCT NOT TESTED.
  4. Step 4: Registered, accredited testing facility (Testing facility) Testing facilities are registered by the Department of Health and must earn ISO/IEC 17025 accreditation within 32 months or lose their registration. Every batch meant for retail sale is tested in final form for potency (THC, plus CBD if labeled, within plus or minus 10%), microbials, mycotoxins, metals, pesticides and solvents.
  5. Step 5: COA and Metrc, by midnight (Testing facility) The facility gives the business a certificate of analysis and must update the tracking system by midnight each day with every sample and result, as a number and a pass or fail. The batch may move only once the COA shows compliance and the tracking system is updated.
  6. Step 6: Fail: remediate or destroy (Department of Health) A failed batch stays in its container under a bold label reading PRODUCT FAILED TESTING. Remediation needs the Department’s approval and is never allowed for metals, pesticides or prohibited solvents; a remediated batch must pass every test again. Otherwise it is destroyed under the approved procedure, logged within one business day and recorded on security cameras.
  7. Step 7: Package + label (Manufacturer) The edible’s marketing layer carries the Department’s standard symbol, a cannabis leaf inside a yellow caution triangle with a black border, at least 1/2 inch square on the front. The symbol rule covers edibles, not flower. The label adds net contents, the testing results and the state warnings in at least 6-point type.
  8. Step 8: Department inspections + state lab (Department of Health) Department of Health inspectors visit dispensaries with a checklist that asks whether every product carries the required warning symbols and labels and whether mandated testing results, including THC in milligrams and percent, appear on all products. The South Dakota Public Health Laboratory is certified for confirmatory testing, and if a failed batch is not handled by the rules, the Department warns every dispensary.

Frequently asked questions

Who tests cannabis in South Dakota?
A cannabis testing facility registered with the South Dakota Department of Health, which must earn ISO/IEC 17025 accreditation within 32 months of registration. Every batch is tested in final form before transfer for potency, microbials, mycotoxins, metals, pesticides and solvents. The facility issues a certificate of analysis and enters each result, with a pass or fail, in Metrc by midnight.
Who pulls the sample in South Dakota?
A designated representative of the testing facility, as state law requires: a person or entity the lab authorizes in writing. The designee needs at least five hours of initial sampling training and three hours each year after, and follows the lab's instructions. The batch is checked and homogenized first, and while results are pending its container is labeled PRODUCT NOT TESTED.
What has to be on a cannabis label in South Dakota?
A South Dakota label shows net contents, the testing results, an expiration date and the state warnings in at least 6-point type, from Contains cannabis to the line that the FDA has not approved the product. Flower adds a not-for-sale-under-21 line, inhalables an under-21 possession line, and edibles the serving size, an onset warning and the yellow triangle symbol.
Do South Dakota edibles have a THC limit?
Yes. An edible other than a tincture, oil or capsule may hold no more than 50 milligrams of THC per serving and 500 milligrams per package. The label gives the serving size and number of servings, and since 1 October 2025 an expiration date no more than 12 months from manufacture.

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Educational information only, not medical advice. Terpene and cannabinoid effects are an active area of research and vary by person, product, and dose. Cannabis is for adults 21+ where legal.

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