No, copies of the CSF and of the EPA stamped approved label are not required to be submitted.
No, Minnesota does not require registration of 2(ee) bulletins. However, 2(ee) bulletins should be submitted to the MDA for review.
No, the required late fee will not be waived. Minnesota law requires an additional fee of 50 percent of the registration application fee to be paid by the applicant for each pesticide to be registered if the application is a renewal application that is submitted after December 31. There are no exceptions. The envelope containing your renewal application must be postmarked by December 31. If it is postmarked January 1 or later, the late fee will be due for each product to be renewed. Only products to be renewed are subject to a late fee.
If you believe that your company has over paid for either a renewal fee or gross sales reporting, please fill out a refund claim form and email it to Pesticide.Registration.MDA@state.mn.us with the subject line “Refund Request”. This form can be found under "Forms + Resources".
Restricted Use Pesticides
No, Minnesota does not classify as Restricted Use any pesticides other than the pesticides classified as Restricted Use by the EPA.
No, Minnesota does not classify as Restricted Use any pesticides other than the pesticides classified as Restricted Use by the EPA.
No, Minnesota does not classify as Restricted Use any pesticides other than the pesticides classified as Restricted Use by the EPA.
If the product is a distributor product, it must meet federal registration/labeling requirements as laid out in the Supplemental distribution code (40 CFR 145.132)
If the product is a distributor product, it must meet federal registration/labeling requirements as laid out in the Supplemental distribution code (40 CFR 145.132)
Labeling must be provided for the following:
- Label of the box/ container
- Individual labels for each product (pesticide or non-pesticide) found inside the box. The active ingredient list found on the box/container referenced above does not count.
- Supplemental labels/pamphlets
According to the Sale and Distribution of Misbranded Pesticides and Devices statute, a person may not offer for sale or distribute a pesticide or device determined by the commissioner to be misbranded, including a pesticide or device that:
- is an imitation of or is offered for sale under the name of another pesticide or device; or
- does not comply with the labeling requirements under this chapter or FIFRA.
The Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA Section 2(p)) defines pesticide “label” and “labeling” as:
- Label: The written, printed, or graphic matter on, or attached to, the pesticide or device or any of its containers or wrappers.
- Labeling: All labels and all other written, printed, or graphic matter accompanying the pesticide or device at any time, or to which reference is made on the label or in literature accompanying the pesticide or device, except to current official publications of the Environmental Protection Agency, the United States Departments of Agriculture and Interior, and the Department of Health and Human Services, State experiment stations, State agricultural colleges, and other similar Federal or State institutions or agencies authorized by law to conduct research in the field of pesticides.
