Lawriter - OAC - 4713-8-04 Standards relating to competent practice as an esthetician.

4713-8-04 Standards relating to competent practice as an esthetician.

(A) An esthetician shall provide cosmetology services within a salon where the license is current, active and appropriate to the scope of practice of esthetics for an esthetician as set forth in section 4713.01 of the Revised Code and the rules of the board.

(B) An esthetician shall maintain knowledge of the duties, responsibilities, and accountabilities of practice and shall practice in accordance with the following:

(1) The laws regulating the practice of esthetics;

(2) The rules of the board;

(3) Any other applicable federal, state, and local laws and rules; and

(4) Position statements, standards for practice, or guidelines for practice from nationally recognized professional esthetic entities; provided these statements, standards, or guidelines are consistent with existing laws or rules.

(C) An esthetician shall demonstrate competence and accountability in all areas of practice in which the esthetician is engaged which includes, but is not limited to, the following:

(1) Consistent performance of all aspects of esthetic services according to acceptable and prevailing standards;

(2) Appropriate recognition, referral or consultation, and intervention, when a complication arises during or after the performance of a specific service or procedure;

(3) The esthetician demonstrates appropriate knowledge, skills, and abilities to provide the cosmetology service, and

(4) The esthetician service does not involve a function or procedure, which is prohibited by any other law or rule and does not exceed the definition of the practice of esthetics in section 4713.01 of the Revised Code.

(D) Estheticians shall not provide any service that claims to have a medical or healing benefit. The scope of practice is limited to beautification , relaxation , and non-invasive services only. The term "therapy" shall only be used with services described in paragraph ( KK) of rule 4713-1-01 of the Administrative Code.

(E) Estheticians may exfoliate stratum corneum cells only. They may use any chemical, mechanical or electrical service to exfoliate cells of the stratum corneum.

(F) Estheticians may use a sterile, single-use, disposable lancet to enhance the opening in a comedo or to create a small opening in the dead surface corneum to facilitate extraction of a milia . Estheticians shall not pierce the stratum corneum or use a lancet for any other purpose. Estheticians shall not perform a comedo enhancement or milia extraction with a lancet unless they have had specific, documented training for the procedure. Used lancets shall be immediately disposed of in a sharps disposal container.

(G) Estheticians working under the direct supervision of a licensed physician shall only provide services within their scope of practice as set forth in Chapter 4713. of the Revised Code and the rules promulgated thereunder.

(H) Chemical peels performed by an esthetician shall be mixed and used at an ingredient concentration of thirty per cent solution or less at final formulation with a pH value not less than three, unless all of the following conditions are met:

(1) The chemical peel preparation is a commercially available product approved for use by cosmetologists and/or estheticians;

(2) The licensee can provide documentation from the manufacturer that the specific product does not penetrate below the stratum corneum when used as directed;

(3) The licensee can provide documentation of training and/or certification in the use of the product;

(4) The licensee follows all manufacturer's directions in the use of the chemical peel preparation; and

(5) The preparation is stored according to the manufacturer's specifications and is discarded after its expiration date.

(I) Estheticians shall not provide services using any device that produces or amplifies electromagnetic radiation at wavelengths equal to or greater than one hundred eighty nanometers .

(J) Estheticians shall not provide services using any device classified as a Class II or Class III medical device by the United States food and drug administration (FDA).

Effective: 2/16/2018
Five Year Review (FYR) Dates: 1/13/2022
Promulgated Under: 119.03
Statutory Authority: 4713.08(A)(20), 4713.08(A)(1)
Rule Amplifies: 4713.01, 4713.35, 4713.15, 4713.14
Prior Effective Dates: 1/10/2004, 3/30/2009, 11/01/2013, 01/13/2017