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Gel Manufacturing: SOP for Labeling Gel Tubes and Jars – V 2.0

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Gel Manufacturing: SOP for Labeling Gel Tubes and Jars – V 2.0

Standard Operating Procedure for Labeling Gel Tubes and Jars in Secondary Packaging


Department Gel Manufacturing
SOP No. SOP/GM/093/2025
Supersedes SOP/GM/093/2022
Page No. Page 1 of 11
Issue Date 02/06/2025
Effective Date 04/06/2025
Review Date 02/06/2026

1. Purpose

To define the process for labeling of gel tubes and jars in accordance with approved labeling specifications, ensuring traceability and compliance with regulatory requirements before secondary packaging.

2. Scope

This procedure applies to all gel products filled into tubes or jars within the Gel Manufacturing department of the pharmaceutical facility.

3.

Responsibilities
  • Packaging Operator: Apply labels correctly and verify each label’s clarity and correctness.
  • Supervisor: Confirm labeling setup, monitor label reconciliation, and escalate issues.
  • Quality Assurance: Conduct in-process checks and approve labeling line before use.

4. Accountability

The Head – Manufacturing is accountable for the integrity and traceability of all labeled gel products.

5. Procedure

5.1 Pre-Labeling Activities

  1. Verify Line Clearance Certificate from QA before starting labeling operations.
  2. Collect labels from the packaging material store against requisition.
  3. Check label details: Product Name, Batch No., Mfg. Date, Exp. Date, MRP, and Regulatory Warnings.
  4. Ensure that label roll orientation matches with labeling machine requirements.

5.2 Setup and Labeling Process

  1. Load the correct label roll into the automatic/semi-automatic labeling machine.
  2. Adjust sensor sensitivity for label gap detection and alignment.
  3. Perform a trial run with 5–10 dummy tubes/jars and inspect for placement accuracy and clarity.
  4. Initiate labeling only after QA clearance.
  5. Feed tubes or jars into the labeling machine and monitor output.
  6. In case of manual labeling, apply the label horizontally without air bubbles or misalignment.
  7. Ensure labels are stuck uniformly without wrinkles or folds.

5.3 Labeling Inspection and Reconciliation

  1. Perform random in-process checks at regular intervals (every 30 minutes) for label position, clarity, and accuracy.
  2. Record results in the Labeling IPC Log Sheet (Annexure-1).
  3. At the end of the batch, count the number of tubes/jars labeled and tally against the label issuance record.
  4. Return excess unused labels to the store with documentation.
  5. Destroy rejected/damaged labels in the presence of QA with proper documentation.

6. Abbreviations

  • IPC: In-Process Control
  • QA: Quality Assurance
  • MRP: Maximum Retail Price
  • SOP: Standard Operating Procedure

7. Documents

  1. Label Issuance Record
  2. Line Clearance Certificate
  3. Labeling IPC Log Sheet – Annexure-1
  4. Label Reconciliation Log

8. References

  • GMP Guidelines – WHO TRS 961 Annex 3
  • Schedule M – Labeling and Packaging Section

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation Jr. Production Chemist QA Executive Head – Manufacturing
Department Gel Manufacturing Quality Assurance Manufacturing

11. Annexures

Annexure-1: Labeling IPC Log Sheet

Time Sample Size Label Text Correctness Positioning Accuracy Comments Checked By
5 Units
5 Units
5 Units

Revision History

Revision Date Revision No. Change Description Reason Approved By
02/06/2022 1.0 Initial version New SOP creation QA Head
02/06/2025 2.0 Added clarity checks and manual labeling section Annual Review QA Head
See also  Gel Manufacturing: SOP for Primary Packaging of Gels - V 2.0
Gels V 2.0 Tags:gel excipients SOP, gel extrudability SOP, gel formulation process guidelines, gel formulation safety SOP, gel formulation SOP template, gel homogenization SOP, gel ingredient weighing SOP, gel labeling and documentation SOP, gel microbial contamination SOP, gel packaging SOP, gel viscosity measurement SOP, gel viscosity testing SOP, pharmaceutical gel SOP, quality control SOP gel formulations, SOP for carbopol gel formulation, SOP for gel pH adjustment, SOP for gel spreadability test, stability testing SOP gel, standard operating procedure gel preparation, topical gel manufacturing SOP

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
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  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Gels V 2.0
  • Injectables V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

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