(215 ILCS 138/1)

Sec. 1.

Short title.

This Act may be cited as the

Uniform Prescription Drug Information Card Act.

(Source: P.A. 91‑777, eff. 1‑1‑01.)

(215 ILCS 138/10)

Sec. 10.

Definitions.

As used in this Act, the following terms have the meanings given in this Section.

"Department" means the Department of Insurance.

"Director" means the Director of Insurance.

"Health benefit plan" means an accident and health insurance policy or certificate subject to the Illinois Insurance Code, a voluntary health services plan subject to the Voluntary Health Services Plans Act, a health maintenance organization subscriber contract subject to the Health Maintenance Organization Act, a plan provided by a multiple employer welfare arrangement, or a plan provided by another benefit arrangement. Without limitation, "health benefit plan" does not mean any of the following types of insurance:

(1) accident;

(2) credit;

(3) disability income;

(4) long‑term or nursing home care;

(5) specified disease;

(6) dental or vision;

(7) coverage issued as a supplement to liability

insurance;

(8) medical payments under automobile or homeowners;

(9) insurance under which benefits are payable with

or without regard to fault as statutorily required to be contained in any liability policy or equivalent self‑insurance;

(10) hospital income or indemnity;

(11) self‑insured health benefit plans under the

federal Employee Retirement Income Security Act of 1974.

(Source: P.A. 91‑777, eff. 1‑1‑01.)

(215 ILCS 138/15)

Sec. 15.

Uniform prescription drug information cards required.

(a) A health benefit plan that issues a card or other technology and provides coverage for prescription drugs or devices and an administrator of such a plan including, but not limited to, third‑party administrators for self‑insured plans and state‑administered plans shall issue to its insureds a card or other technology containing uniform prescription drug information. The uniform prescription drug information card or other technology shall specifically identify and display the following mandatory data elements on the front of the card:

(1) BIN number;

(2) Processor control number if required for claims

adjudication;

(3) Group number;

(4) Card issuer identifier;

(5) Cardholder ID number; and

(6) Cardholder name.

The uniform prescription drug information card or other technology shall specifically identify and display the following mandatory data elements on the back of the card:

(1) Claims submission names and addresses; and

(2) Help desk telephone numbers and names.

(b) A new uniform prescription drug information card or other technology shall be issued by a health benefit plan upon enrollment and reissued upon any change in the insured's coverage that affects mandatory data elements contained on the card.

(Source: P.A. 91‑777, eff. 1‑1‑01.)

(215 ILCS 138/20)

Sec. 20.

Applicability and enforcement.

(a) This Act applies to health benefit plans that are amended, delivered, issued, or renewed on and after the effective date of this amendatory Act of the 91st General Assembly.

(b) The Director may adopt rules necessary to implement the Department's responsibilities under this Act. To enforce the provisions of this Act, the Director may issue a cease and desist order or require a health benefit plan to submit a plan of correction for violations of this Act, or both. Subject to the provisions of the Illinois Administrative Procedure Act, the Director may, pursuant to Section 403A of the Illinois Insurance Code, impose upon a health benefit plan an administrative fine not to exceed $250,000 for failure to submit a requested plan of correction, failure to comply with its plan or correction, or repeated violations of this Act.

(Source: P.A. 91‑777, eff. 1‑1‑01.)

(215 ILCS 138/5)

Sec. 5.

Legislative intent.

It is the intent of the legislature to lessen patients' waiting times, decrease administrative burdens for pharmacies, and improve care to patients by minimizing confusion, eliminating unnecessary paperwork, and streamlining the dispensing of prescription products paid for by third‑party payors. This Act shall be broadly applied and interpreted to effectuate this purpose.

(Source: P.A. 91‑777, eff. 1‑1‑01.)

(215 ILCS 138/99)

Sec. 99.

Effective date.

This Act takes effect on January 1, 2001.

(Source: P.A. 91‑777, eff. 1‑1‑01.)