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SF 1752
Minnesota Senate•Introduced
Summary
SF 1752, “Coverage of over-the-counter contraceptive, drugs, devices, and products requirement by insurers and medical assistance”, was introduced in the Senate on Feb 24, 2025 by Sen. Lindsey Port (D) with 4 co-sponsors. It was referred to Commerce and Consumer Protection, and last saw action on Feb 27, 2025: Authors added Johnson Stewart; Mitchell.
Record
Text
SF 1752 has 4 co-sponsors.
sf1752/introduced.txt01/29/25 REVISOR RSI/HL 25-02425 as introducedSENATESTATE OF MINNESOTANINETY-FOURTH SESSION S.F. No. 1752(SENATE AUTHORS: PORT, Maye Quade, Mann, Johnson Stewart and Mitchell)DATE D-PG OFFICIAL STATUS02/24/2025 473 Introduction and first readingReferred to Commerce and Consumer Protection02/27/2025 580 Authors added Johnson Stewart; Mitchell1.1A bill for an act1.2relating to health insurance; requiring coverage of over-the-counter contraceptive1.3drugs, devices, and products by insurers and medical assistance; requiring reports;1.4amending Minnesota Statutes 2024, sections 62Q.522, subdivisions 1, 2;1.5256B.0625, subdivision 13.1.6 BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:1.7Section 1. Minnesota Statutes 2024, section 62Q.522, subdivision 1, is amended to read:1.8Subdivision 1. Definitions. (a) The definitions in this subdivision apply to this section.1.9(b) "Contraceptive method" means a drug, device, or other product approved by the1.10 Food and Drug Administration to prevent unintended pregnancy prescription contraceptive1.11 or over-the-counter contraceptive.1.12(c) "Contraceptive service" or "service" means consultation, examination, procedures,1.13 and medical services related to the prevention of unintended pregnancy, excluding1.14 vasectomies. This includes but is not limited to voluntary sterilization procedures, patient1.15 education, counseling on contraceptives, and follow-up services related to contraceptive1.16 methods or services, management of side effects, counseling for continued adherence, and1.17 device insertion or removal.1.18(d) "Medical necessity" includes but is not limited to considerations such as severity of1.19 side effects, difference in permanence and reversibility of a contraceptive method or service,1.20 and ability to adhere to the appropriate use of the contraceptive method or service, as1.21 determined by the attending provider.1.22(e) "Over-the-counter contraceptive" or "OTC contraceptive" means a drug, device, or1.23 other product that:Section 1. 101/29/25 REVISOR RSI/HL 25-02425 as introduced2.1 (1) is approved by the Food and Drug Administration to prevent unintended pregnancy;2.2 and2.3 (2) does not require a prescription.2.4 (f) "Pharmacy" has the meaning given in section 151.01.2.5 (g) "Prescription contraceptive" means a drug, device, or other product that:2.6 (1) is approved by the Food and Drug Administration to prevent unintended pregnancy;2.7 and2.8 (2) requires a prescription.2.9 (e) (h) "Therapeutic equivalent version" means a drug, device, or product that can be2.10 expected to have the same clinical effect and safety profile when administered to a patient2.11 under the conditions specified in the labeling, and that:2.12 (1) is approved as safe and effective;2.13 (2) is a pharmaceutical equivalent: (i) containing identical amounts of the same active2.14 drug ingredient in the same dosage form and route of administration; and (ii) meeting2.15 compendial or other applicable standards of strength, quality, purity, and identity;2.16 (3) is bioequivalent in that:2.17 (i) the drug, device, or product does not present a known or potential bioequivalence2.18 problem and meets an acceptable in vitro standard; or2.19 (ii) if the drug, device, or product does present a known or potential bioequivalence2.20 problem, it is shown to meet an appropriate bioequivalence standard;2.21 (4) is adequately labeled; and2.22 (5) is manufactured in compliance with current manufacturing practice regulations.2.23 EFFECTIVE DATE. This section is effective January 1, 2026, and applies to health2.24 plans offered, issued, or renewed on or after that date.2.25 Sec. 2. Minnesota Statutes 2024, section 62Q.522, subdivision 2, is amended to read:2.26 Subd. 2. Required coverage; cost sharing prohibited. (a) A health plan must provide2.27 coverage for contraceptive methods and services.2.28 (b) A health plan company must not impose cost-sharing requirements, including co-pays,2.29 deductibles, or coinsurance, for contraceptive methods or services.Sec. 2. 201/29/25 REVISOR RSI/HL 25-02425 as introduced3.1 (c) A health plan company must not impose any referral requirements, restrictions, or3.2 delays for contraceptive methods or services.3.3 (d) A health plan must include at least one of each type of Food and Drug Administration3.4 approved contraceptive method in its formulary. Subject to paragraph (g), if more than one3.5 therapeutic equivalent version of a contraceptive method is approved, a health plan must3.6 include at least one therapeutic equivalent version in its formulary, but is not required to3.7 include all therapeutic equivalent versions.3.8 (e) For each health plan, a health plan company must list the contraceptive methods and3.9 services that are covered without cost-sharing in a manner that is easily accessible to3.10 enrollees, health care providers, and representatives of health care providers. The list for3.11 each health plan must be promptly updated to reflect changes to the coverage.3.12 (f) If an enrollee's attending provider recommends a particular contraceptive method or3.13 service based on a determination of medical necessity for that enrollee, the health plan must3.14 cover that contraceptive method or service without cost-sharing. The health plan company3.15 issuing the health plan must defer to the attending provider's determination that the particular3.16 contraceptive method or service is medically necessary for the enrollee.3.17 (g) Notwithstanding paragraph (d), a health plan must cover all types and brands of OTC3.18 contraceptives purchased at a pharmacy without requiring a prescription.3.19 (h) A health plan must cover all OTC contraceptives purchased at a pharmacy at the3.20 point-of-sale without requiring a prescription.3.21 (i) A health plan must not limit the type, quantity, or purchase frequency, and must not3.22 impose any restriction or requirement, based on prescription status of OTC contraceptives3.23 purchased at a pharmacy.3.24 (j) If the application of this subdivision before an enrollee has met the enrollee's health3.25 plan's deductible results in: (1) health savings account ineligibility under United States3.26 Code, title 26, section 223; or (2) catastrophic health plan ineligibility under United States3.27 Code, title 42, section 18022(e), then this subdivision applies to contraceptive methods and3.28 services only after the enrollee has met the enrollee's health plan's deductible.3.29 EFFECTIVE DATE. This section is effective January 1, 2026, and applies to health3.30 plans offered, issued, or renewed on or after that date.Sec. 2. 301/29/25 REVISOR RSI/HL 25-02425 as introduced4.1 Sec. 3. Minnesota Statutes 2024, section 256B.0625, subdivision 13, is amended to read:4.2 Subd. 13. Drugs. (a) Medical assistance covers drugs, except for fertility drugs when4.3 specifically used to enhance fertility, if prescribed by a licensed practitioner and dispensed4.4 by a licensed pharmacist, by a physician enrolled in the medical assistance program as a4.5 dispensing physician, or by a physician, a physician assistant, or an advanced practice4.6 registered nurse employed by or under contract with a community health board as defined4.7 in section 145A.02, subdivision 5, for the purposes of communicable disease control.4.8 (b) The dispensed quantity of a prescription drug must not exceed a 34-day supply unless4.9 authorized by the commissioner or as provided in paragraph (h) or the drug appears on the4.10 90-day supply list published by the commissioner. The 90-day supply list shall be published4.11 by the commissioner on the department's website. The commissioner may add to, delete4.12 from, and otherwise modify the 90-day supply list after providing public notice and the4.13 opportunity for a 15-day public comment period. The 90-day supply list may include4.14 cost-effective generic drugs and shall not include controlled substances.4.15 (c) For the purpose of this subdivision and subdivision 13d, an "active pharmaceutical4.16 ingredient" is defined as a substance that is represented for use in a drug and when used in4.17 the manufacturing, processing, or packaging of a drug becomes an active ingredient of the4.18 drug product. An "excipient" is defined as an inert substance used as a diluent or vehicle4.19 for a drug. The commissioner shall establish a list of active pharmaceutical ingredients and4.20 excipients which are included in the medical assistance formulary. Medical assistance covers4.21 selected active pharmaceutical ingredients and excipients used in compounded prescriptions4.22 when the compounded combination is specifically approved by the commissioner or when4.23 a commercially available product:4.24 (1) is not a therapeutic option for the patient;4.25 (2) does not exist in the same combination of active ingredients in the same strengths4.26 as the compounded prescription; and4.27 (3) cannot be used in place of the active pharmaceutical ingredient in the compounded4.28 prescription.4.29 (d) Medical assistance covers the following over-the-counter drugs:4.30 (1) when prescribed by a licensed practitioner or by a licensed pharmacist who meets4.31 standards established by the commissioner, in consultation with the board of pharmacy:4.32 (i) antacids,;4.33 (ii) acetaminophen,;Sec. 3. 401/29/25 REVISOR RSI/HL 25-02425 as introduced5.1 (iii) family planning products,;5.2 (iv) aspirin,;5.3 (v) insulin,;5.4 (vi) products for the treatment of lice,;5.5 (vii) vitamins for adults with documented vitamin deficiencies,;5.6 (viii) vitamins for children under the age of seven and pregnant or nursing women,; and5.7 (ix) any other over-the-counter drug identified by the commissioner, in consultation5.8 with the Formulary Committee, as necessary, appropriate, and cost-effective for the treatment5.9 of certain specified chronic diseases, conditions, or disorders,; and this5.10 (2) all over-the-counter contraceptives, as defined in section 62Q.522, regardless of5.11 whether the drug has been prescribed.5.12 A determination shall by the commissioner under clause (1), item (ix), is not be subject to5.13 the requirements of chapter 14. A pharmacist may prescribe over-the-counter medications5.14 as provided under this paragraph for purposes of receiving reimbursement under Medicaid.5.15 When prescribing over-the-counter drugs under this paragraph, licensed pharmacists must5.16 consult with the recipient to determine necessity, provide drug counseling, review drug5.17 therapy for potential adverse interactions, and make referrals as needed to other health care5.18 professionals.5.19 (e) Effective January 1, 2006, medical assistance shall not cover drugs that are coverable5.20 under Medicare Part D as defined in the Medicare Prescription Drug, Improvement, and5.21 Modernization Act of 2003, Public Law 108-173, section 1860D-2(e), for individuals eligible5.22 for drug coverage as defined in the Medicare Prescription Drug, Improvement, and5.23 Modernization Act of 2003, Public Law 108-173, section 1860D-1(a)(3)(A). For these5.24 individuals, medical assistance may cover drugs from the drug classes listed in United States5.25 Code, title 42, section 1396r-8(d)(2), subject to this subdivision and subdivisions 13a to5.26 13g, except that drugs listed in United States Code, title 42, section 1396r-8(d)(2)(E), shall5.27 not be covered.5.28 (f) Medical assistance covers drugs acquired through the federal 340B Drug Pricing5.29 Program and dispensed by 340B covered entities and ambulatory pharmacies under common5.30 ownership of the 340B covered entity. Medical assistance does not cover drugs acquired5.31 through the federal 340B Drug Pricing Program and dispensed by 340B contract pharmacies.Sec. 3. 501/29/25 REVISOR RSI/HL 25-02425 as introduced6.1 (g) Notwithstanding paragraph (a), medical assistance covers self-administered hormonal6.2 contraceptives prescribed and dispensed by a licensed pharmacist in accordance with section6.3 151.37, subdivision 14; nicotine replacement medications prescribed and dispensed by a6.4 licensed pharmacist in accordance with section 151.37, subdivision 15; and opiate antagonists6.5 used for the treatment of an acute opiate overdose prescribed and dispensed by a licensed6.6 pharmacist in accordance with section 151.37, subdivision 16.6.7 (h) Medical assistance coverage for a prescription contraceptive must provide a 12-month6.8 supply for any prescription contraceptive if a 12-month supply is prescribed by the6.9 prescribing health care provider. The prescribing health care provider must determine the6.10 appropriate duration for which to prescribe the prescription contraceptives, up to 12 months.6.11 For purposes of this paragraph, "prescription contraceptive" means any drug or device that6.12 requires a prescription and is approved by the Food and Drug Administration to prevent6.13 pregnancy. Prescription contraceptive does not include an emergency contraceptive drug6.14 approved to prevent pregnancy when administered after sexual contact. For purposes of this6.15 paragraph, "health plan" has the meaning provided in section 62Q.01, subdivision 3.6.16 EFFECTIVE DATE. This section is effective January 1, 2026.6.17 Sec. 4. OUTREACH AND REPORTS.6.18 (a) The Department of Commerce must work with the Departments of Health and Human6.19 Services to provide public information about over-the-counter contraception coverage.6.20 (b) The Department of Commerce must work with the Departments of Health and Human6.21 Services and provide a report by March 31, 2027, and annually thereafter, to the standing6.22 committees of the legislature with oversight of issues relating to commerce, health, and6.23 human services. The report must include information and data regarding the use of coverage6.24 and related costs to health plans and the state to provide over-the-counter contraceptives.Sec. 4. 6
Coverage of over-the-counter contraceptive, drugs, devices, and products requirement by insurers and medical assistance
Sponsors
Sen. Lindsey Port (D) sponsors SF 1752, and 4 members have co-sponsored it.
Committees
SF 1752 went before 1 committee: Commerce and Consumer Protection.
History
SF 1752 has taken 3 actions since Feb 24, 2025, the latest on Feb 27, 2025.
| Chamber | Action | |||
|---|---|---|---|---|
Feb 27, 2025 | Senate | Authors added Johnson Stewart; Mitchell | ||
Feb 24, 2025 | Senate | Introduction and first reading | ||
Feb 24, 2025 | Senate | Referred to Commerce and Consumer Protection |
Votes
SF 1752 has not gone to a roll call.
Source: revisor.mn.gov · legiscan.com