Effective: March 20, 2013
Latest Legislation: House Bill 334 - 129th General Assembly
(A) As used in this section and sections 3715.051 to 3715.054 and 3715.06 of the Revised Code:
(1) "Consumer product" means any food or drink that is consumed or used by humans and any drug, including a drug that may be provided legally only pursuant to a prescription, that is intended to be consumed or used by humans.
(2) "Drug," "licensed health professional authorized to prescribe drugs," "pharmacy," "prescriber," "prescription," and "terminal distributor of dangerous drugs" have the same meanings as in section 4729.01 of the Revised Code.
(3) "Ephedrine" means any material, compound, mixture, or preparation that contains any quantity of ephedrine, any of its salts, optical isomers, or salts of optical isomers.
(4) "Ephedrine product" means a consumer product that contains ephedrine.
(5) "Law enforcement official" means an officer or employee of any agency or authority of the United States, a state, a territory, a political subdivision of a state or territory, or an Indian tribe, who is empowered by the law to investigate or conduct an official inquiry into a potential violation of law or prosecute or otherwise conduct a criminal, civil, or administrative proceeding arising from an alleged violation of law.
(6) "National precursor log exchange" or "exchange" means the electronic system for tracking sales of pseudoephedrine products and ephedrine products on a national basis that is administered by the national association of drug diversion investigators or a successor organization.
(7) "Pharmacist" means a person licensed under Chapter 4729. of the Revised Code to engage in the practice of pharmacy.
(8) "Proof of age" means a driver's license, a commercial driver's license, a military identification card, a passport, or an identification card issued under sections 4507.50 to 4507.52 of the Revised Code that shows a person is eighteen years of age or older.
(9) "Pseudoephedrine" means any material, compound, mixture, or preparation that contains any quantity of pseudoephedrine, any of its salts, optical isomers, or salts of optical isomers.
(10) "Pseudoephedrine product" means a consumer product that contains pseudoephedrine.
(11) "Retailer" means a place of business that offers consumer products for sale to the general public.
(12) "Single-ingredient preparation" means a compound, mixture, preparation, or substance that contains a single active ingredient.
(13) "Stop-sale alert" means a notification sent from the national precursor log exchange to a retailer or terminal distributor of dangerous drugs indicating that the completion of a sale of a pseudoephedrine product or ephedrine product would result in a violation of division (A)(1) of section 2925.56 of the Revised Code or federal law.
(14) "Wholesaler" has the same meaning as in section 3719.01 of the Revised Code.
(B) A retailer or terminal distributor of dangerous drugs that sells, offers to sell, holds for sale, delivers, or otherwise provides a pseudoephedrine product or ephedrine product to the public shall do all of the following:
(1) Segregate pseudoephedrine products or ephedrine products from other merchandise so that no member of the public may procure or purchase such products without the direct assistance of a pharmacist or other authorized employee of the retailer or terminal distributor of dangerous drugs;
(2) With regard to each time a pseudoephedrine product or ephedrine product is sold or otherwise provided without a valid prescription:
(a) Determine, by examination of a valid proof of age, that the purchaser or recipient is at least eighteen years of age;
(b) Using any information available, including information from the national precursor log exchange if the information is accessible, make a reasonable attempt to ensure that no individual purchases or receives an amount of pseudoephedrine product or ephedrine product that is greater than either of the following:
(i) Three and six tenths grams within a period of a single day;
(ii) Nine grams within a period of thirty consecutive days.
The maximum amounts specified in divisions (B)(2)(b)(i) and (ii) of this section apply to the total amount of base pseudoephedrine or base ephedrine in the pseudoephedrine product or ephedrine product, respectively. The maximum amounts do not apply to the product's overall weight.
(3) Maintain a log book of pseudoephedrine product or ephedrine product purchases, in accordance with section 3715.051 of the Revised Code;
(4) If required to comply with section 3715.052 of the Revised Code, submit the information specified in divisions (A)(1)(a) to (d) of that section to the national precursor log exchange.
(C) Prescriptions, orders, and records maintained pursuant to this section and stocks of pseudoephedrine products and ephedrine products shall be open for inspection to federal, state, county, and municipal officers, and employees of the state board of pharmacy whose duty it is to enforce the laws of this state or of the United States relating to controlled substances. Such prescriptions, orders, records, and stocks shall be open for inspection by the state medical board and its employees for purposes of enforcing Chapter 4731. of the Revised Code.
Structure Ohio Revised Code
Title 37 | Health-Safety-Morals
Chapter 3715 | Pure Food and Drug Law
Section 3715.01 | Pure Food and Drug Law Definitions.
Section 3715.011 | Effect of Changes to Federal Law.
Section 3715.02 | Definitions for Food or Class of Food and Standards.
Section 3715.021 | Standards and Good Manufacturing Practices for Food Processing Establishments.
Section 3715.022 | Standards for Food Sampling and Procedures for Administration.
Section 3715.023 | Labels for Cottage Food Production Operation, Processor, or Beekeeper.
Section 3715.024 | Voluntary Inspection of Processor's or Beekeeper's Facilities.
Section 3715.025 | Restrictions on Cottage Food Production Operation.
Section 3715.03 | Right of Entry.
Section 3715.04 | Certificate of Health and Freesale - Inspection - Fee.
Section 3715.041 | Registration of Food Processing Establishments.
Section 3715.05 | Sale of Pseudoephedrine or Ephedrine Product.
Section 3715.051 | Log of All Purchases of Pseudoephedrine or Ephedrine Products.
Section 3715.053 | Exemptions.
Section 3715.054 | Liability for Damages Due to Sale of Pseudoephedrine or Ephedrine Products.
Section 3715.06 | Discovery of Theft or Loss of Pseudoephedrine Product.
Section 3715.07 | Standards for Flavoring Extracts.
Section 3715.13 | Sale of Diphtheria Antitoxin.
Section 3715.14 | Prohibition Against Sale of Unlabeled Canned Fruits and Vegetables by a Dealer.
Section 3715.16 | Prohibition Against Falsely Labeling Fruit or Vegetable Packages.
Section 3715.17 | Prohibition Against Selling Falsely Labeled Fruit or Vegetables.
Section 3715.171 | Date Labels for Perishable Foods.
Section 3715.18 | Manufacturer or Packer Must Attach Label to Soaked Goods.
Section 3715.19 | Vendor Must Attach Label to Soaked Goods.
Section 3715.20 | Prosecution.
Section 3715.23 | Manufacture and Sale of Adulterated Candy - Sample for Analysis.
Section 3715.24 | Maple Product Standards and Grades.
Section 3715.25 | Prohibited Acts Regarding Maple Products.
Section 3715.27 | Cider Manufacturing and Labeling.
Section 3715.29 | Cider or Apple Vinegar.
Section 3715.30 | Wine or Grape Vinegar.
Section 3715.31 | Malt Vinegar.
Section 3715.32 | Distilled Vinegar.
Section 3715.33 | Fermented Vinegar.
Section 3715.34 | Injurious Ingredients in Vinegar - Brands.
Section 3715.35 | Brands on Casks of Cider Vinegar.
Section 3715.36 | Prohibition Against Selling Vinegar Not Made or Branded in Compliance With Law.
Section 3715.37 | Branding of Cider Vinegar by Manufacturing Farmer.
Section 3715.38 | Prohibitions Regarding Honey.
Section 3715.52 | Prohibited Acts.
Section 3715.53 | Injunctions.
Section 3715.54 | Exceptions to Liability.
Section 3715.55 | Notice of Adulteration, Misbranding, or Expiration.
Section 3715.551 | Embargo of Food.
Section 3715.57 | Written Notice or Warning for Minor Violations Sufficient.
Section 3715.59 | When Food Is Adulterated.
Section 3715.60 | Misbranded Food.
Section 3715.61 | Director of Agriculture - Powers Regarding Permits.
Section 3715.62 | Unsafe Food.
Section 3715.63 | When Drug or Device Is Adulterated.
Section 3715.64 | Misbranded Drug or Device.
Section 3715.65 | Application for New Drug Required.
Section 3715.66 | Adulterated Cosmetics.
Section 3715.67 | Misbranded Cosmetics.
Section 3715.68 | False or Misleading Advertisement.
Section 3715.69 | Adoption of Rules for Enforcement.
Section 3715.70 | Right of Entry - Examination of Samples.
Section 3715.71 | Publication of Reports - Dissemination of Information.
Section 3715.72 | Administrative Procedure - Exceptions.
Section 3715.73 | Fines or Forfeited Bonds to Be Paid Into State Treasury.
Section 3715.74 | Governor May Declare Adulterated Consumer Product Emergency.
Section 3715.80 | Dietary Supplement Defined.
Section 3715.81 | Dietary Supplement to Be Treated as a Food.
Section 3715.82 | Adoption of Rules.
Section 3715.83 | Dietary Supplement Considered to Be Adulterated.
Section 3715.84 | Requirements for Labeling - Misbranding.
Section 3715.85 | Publication Used in Connection With Sale to Consumers of Dietary Supplement.
Section 3715.86 | Dietary Supplement Not Considered Food Additive.
Section 3715.87 | Drug Repository Program for Donated Prescription Drugs - Definitions.
Section 3715.873 | Adoption of Rules.
Section 3715.88 | Dangerous Drug Donation Definitions.
Section 3715.89 | Dangerous Drug Donation Requirements.
Section 3715.90 | Pharmacy School Acceptance of Dangerous Drug Donations.
Section 3715.91 | Dangerous Drug Donation Implementing Rules.
Section 3715.92 | Immunity of Pharmacy School Accepting Dangerous Drugs.