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410h — Puerto Rico Law | CourtGPT
  1. Home/
  2. Laws/
  3. Puerto Rico/
  4. Title Twenty - Examining Boards and Professional Colleges (§§ 1 — 6033)/
  5. Chapter 20 - Pharmacy Sub/
  6. Subchapter V - Manufacture, Distribution and Dispensation of Medications § 410 - Medication Register/
  7. 410h
Puerto Rico Legal Code

410h

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Any retail nonprescription medication distributor shall apply for and obtain a license authorizing him/her to sell nonprescription drugs as provided for in this chapter and its regulations. Together with the application for the register certificate, a listing of the nonprescription medications he/she distributes shall be included.Said medications shall be kept and sold in their original packages, duly labeled by the manufacturer, and shall be kept in an environment and at a temperature which are appropriate for preserving their quality, purity and potency, pursuant to the manufacturer’s specifications. History —Sept. 3, 2004, No. 247, § 5.09.

Any retail nonprescription medication distributor shall apply for and obtain a license authorizing him/her to sell nonprescription drugs as provided for in this chapter and its regulations. Together with the application for the register certificate, a listing of the nonprescription medications he/she distributes shall be included.Said medications shall be kept and sold in their original packages, duly labeled by the manufacturer, and shall be kept in an environment and at a temperature which are appropriate for preserving their quality, purity and potency, pursuant to the manufacturer’s specifications. History —Sept. 3, 2004, No. 247, § 5.09.

Any retail nonprescription medication distributor shall apply for and obtain a license authorizing him/her to sell nonprescription drugs as provided for in this chapter and its regulations. Together with the application for the register certificate, a listing of the nonprescription medications he/she distributes shall be included.Said medications shall be kept and sold in their original packages, duly labeled by the manufacturer, and shall be kept in an environment and at a temperature which are appropriate for preserving their quality, purity and potency, pursuant to the manufacturer’s specifications. History —Sept. 3, 2004, No. 247, § 5.09.