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Elixir Department: SOP for Addition of Volatile and Flavoring Agents – V 2.0

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Elixir Department: SOP for Addition of Volatile and Flavoring Agents – V 2.0

Standard Operating Procedure for Addition of Volatile and Flavoring Agents in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/062/2025
Supersedes SOP/ELX/062/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To define the procedure for the controlled addition of volatile ingredients and flavoring agents in elixir manufacturing to maintain sensory quality, dosage uniformity, and product stability.

2. Scope

This SOP applies to the addition of volatile solvents (e.g., ethanol) and flavoring substances (natural or artificial) to elixir batches manufactured in the Elixir Department.

3. Responsibilities

  • Production Operator:
    • Handle and add volatile/flavoring agents per BMR instructions.
    • Ensure closed-system transfer where applicable.
  • Production Supervisor:
    • Verify material identity, addition quantity, and compliance with safety protocols.
  • QA Officer:
    • Monitor handling and addition process, and sign off final verification.
See also  Elixir Department: SOP for Controlled Substance Dispensing for Elixirs - V 2.0

4. Accountability

The Production Head is accountable for ensuring that volatile and flavoring agents are added under controlled conditions and in accordance with the BMR.

5. Procedure

5.1 Pre-Addition Requirements

  1. Ensure batch mixing is complete
and the solution is cooled to below 30°C before addition of volatile/flavoring agents.
  • Check and confirm the material labels, batch numbers, and expiry dates against the BMR.
  • Transfer materials to the manufacturing area only after QA release.
  • 5.2 Addition Procedure

    1. Use a closed funnel or peristaltic pump to add volatile agents (e.g., ethanol) to prevent evaporation loss.
    2. Introduce flavoring agents directly into the vortex of the agitating batch.
    3. Continue mixing at moderate speed (50–80 RPM) for a minimum of 15 minutes post-addition.
    4. Ensure the tank lid is closed throughout the process to reduce volatilization.

    5.3 Safety Measures

    1. Use PPE (gloves, mask, goggles) while handling alcohol-based or volatile ingredients.
    2. Ensure local exhaust ventilation is operational in the addition area.
    3. Avoid open flames or sources of ignition in proximity to the materials.

    5.4 Documentation

    1. Enter details of quantity, time, temperature, and material in the Flavor & Volatile Addition Log (Annexure-1).
    2. Cross-verify with supervisor and attach to the BMR.

    6. Abbreviations

    • SOP: Standard Operating Procedure
    • BMR: Batch Manufacturing Record
    • QA: Quality Assurance
    • PPE: Personal Protective Equipment

    7. Documents

    1. Flavor & Volatile Addition Log (Annexure-1)
    2. Batch Manufacturing Record
    3. Material Usage Authorization Form (Annexure-2)

    8. References

    • WHO TRS 961 Annex 3 – GMP Guidelines for Pharmaceutical Liquids
    • 21 CFR 211.113 – Control of Microbial Contamination

    9. SOP Version

    Version: 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Flavor & Volatile Addition Log

    Date Batch No. Material Name Quantity (mL) Time of Addition Temperature (°C) Added By Verified By
    11/04/2025 ELX-1008 Orange Flavor 150 11:30 AM 28 Rajesh Kumar Sunita Reddy
    11/04/2025 ELX-1008 Ethanol IP 500 11:45 AM 28 Rajesh Kumar Sunita Reddy

    Annexure-2: Material Usage Authorization Form

    Date Material Batch No. Approved Quantity Authorized By Remarks
    11/04/2025 Ethanol IP ETH/0425 500 mL Manju Sharma For Batch ELX-1008

    Revision History:

    Revision Date Revision No. Revision Details Reason for Revision Approved By
    01/01/2024 1.0 Initial Issue New SOP QA Head
    11/04/2025 2.0 Added Closed System and Safety Instructions Process Safety Update QA Head
    See also  Elixir Department: SOP for Handling Material Return Post Dispensing - V 2.0
    Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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    NEW! Revised SOPs – V 2.0

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