Title
Regulation of Virus and Serum Sales
Law
Act No. 3073
Decision Date
Mar 16, 1923
A 1923 Philippine law regulates the sale of medical products, requiring licenses, proper labeling, and inspections to protect public health, with violations punishable by fines or imprisonment.

Law Summary

Prohibition on Label Falsification and Tampering

  • Strict ban on falsifying, relabeling, or remarking packages or containers.
  • Prohibition against altering labels or marks to misrepresent the contents.

Authorized Inspections for Public Health Safeguarding

  • Empowerment of authorized officers, agents, or employees of the Bureau of Health to enter and inspect establishments.
  • Inspections relate to the propagation and preparation of regulated products intended for sale or international shipment to ensure compliance.

Creation and Powers of the Regulatory Board

  • Establishment of a board composed of the Secretary of Public Instruction (chairman), Director of Health, and Director of Bureau of Science.
  • Board authorized to promulgate rules governing licensing, suspension, and revocation procedures.
  • Licenses granted conditionally on the right of inspection of foreign manufacturing establishments.
  • Applications for licenses to be submitted to the Secretary of Public Instruction who oversees issuance based on Director of Health’s recommendations.

Prohibition Against Interference with Government Officers

  • Illegal to obstruct or interfere with government officials performing duties under the Act or its regulations.

Penalties for Violations

  • Violators subject to penalties including fines up to one thousand pesos, imprisonment up to one year, or both, at the court’s discretion.

Effectivity

  • The Act takes effect upon its approval, establishing immediate legal force and effect.

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